LOCUS       XM_047420684             704 bp    mRNA    linear   PRI 25-AUG-2024
DEFINITION  PREDICTED: Homo sapiens replication factor C subunit 2 (RFC2),
            transcript variant X2, mRNA.
ACCESSION   XM_047420684
VERSION     XM_047420684.1
DBLINK      BioProject: PRJNA168
KEYWORDS    RefSeq.
SOURCE      Homo sapiens (human)
  ORGANISM  Homo sapiens
            Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
            Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini;
            Catarrhini; Hominidae; Homo.
COMMENT     MODEL REFSEQ:  This record is predicted by automated computational
            analysis. This record is derived from a genomic sequence
            (NC_000007.14) annotated using gene prediction method: Gnomon,
            supported by EST evidence.
            Also see:
                Documentation of NCBI's Annotation Process
            
            ##Genome-Annotation-Data-START##
            Annotation Provider         :: NCBI RefSeq
            Annotation Status           :: Updated annotation
            Annotation Name             :: GCF_000001405.40-RS_2024_08
            Annotation Pipeline         :: NCBI eukaryotic genome annotation
                                           pipeline
            Annotation Software Version :: 10.3
            Annotation Method           :: Best-placed RefSeq; Gnomon;
                                           RefSeqFE; cmsearch; tRNAscan-SE
            Features Annotated          :: Gene; mRNA; CDS; ncRNA
            Annotation Date             :: 08/23/2024
            ##Genome-Annotation-Data-END##
FEATURES             Location/Qualifiers
     source          1..704
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="7"
     gene            1..704
                     /gene="RFC2"
                     /gene_synonym="RFC40"
                     /note="replication factor C subunit 2; Derived by
                     automated computational analysis using gene prediction
                     method: Gnomon. Supporting evidence includes similarity
                     to: 24 ESTs, 20 long SRA reads, and 100% coverage of the
                     annotated genomic feature by RNAseq alignments, including
                     73 samples with support for all annotated introns"
                     /db_xref="GeneID:5982"
                     /db_xref="HGNC:HGNC:9970"
                     /db_xref="MIM:600404"
     CDS             17..598
                     /gene="RFC2"
                     /gene_synonym="RFC40"
                     /codon_start=1
                     /product="replication factor C subunit 2 isoform X2"
                     /protein_id="XP_047276640.1"
                     /db_xref="GeneID:5982"
                     /db_xref="HGNC:HGNC:9970"
                     /db_xref="MIM:600404"
                     /translation="MEVEAVCGGAGEVEAQDSDPAPAFSKAPGSAGHYELPWVEKYRP
                     VKLNEIVGNEDTVSRLEVFAREGNVPNIIIAGPPGTGKTTSILCLARALLGPALKDAM
                     LELNASNDRGIDVVRNKIKMFAQQKVTLPKGRHKIIILDEADSMTDGAQQALRRTMEI
                     YSKTTRFALACNASDKIIGAEQPAVHLLRIWLH"
ORIGIN      
        1 aagaggaggc gcgagaatgg aggtggaggc cgtctgtggt ggcgcgggcg aggtggaggc
       61 ccaggactct gaccctgccc ctgccttcag caaggccccc ggcagcgccg gccactacga
      121 actgccgtgg gttgaaaaat ataggccagt aaagctgaat gaaattgtcg ggaatgaaga
      181 caccgtgagc aggctagagg tctttgcaag ggaaggaaat gtgcccaaca tcatcattgc
      241 gggccctcca ggaaccggca agaccacaag cattctgtgc ttggcccggg ccctgctggg
      301 cccagcactc aaagatgcca tgttggaact caatgcttca aatgacaggg gcattgacgt
      361 tgtgaggaat aaaattaaaa tgtttgctca acaaaaagtc actcttccca aaggccgaca
      421 taagatcatc attctggatg aagcagacag catgaccgac ggagcccagc aagccttgag
      481 gagaaccatg gaaatctact ctaaaaccac tcgcttcgcc cttgcttgta atgcttcgga
      541 taagatcatc ggcgctgaac aacctgcagt ccaccttctc aggatttggc ttcattaaca
      601 gtgagaacgt gttcaaggtc tgtgacgagc cccacccact gctggtaaag gagatgatcc
      661 agcactgtgt gaatgccaac attgacgaag cctacaaggt tggc
//
