LOCUS       NM_001396027             696 bp    mRNA    linear   PRI 16-APR-2022
DEFINITION  Homo sapiens family with sequence similarity 246 member C
            (gene/pseudogene) (FAM246C), mRNA.
ACCESSION   NM_001396027
VERSION     NM_001396027.1
KEYWORDS    RefSeq; RefSeq Select.
SOURCE      Homo sapiens (human)
  ORGANISM  Homo sapiens
            Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
            Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini;
            Catarrhini; Hominidae; Homo.
COMMENT     VALIDATED REFSEQ: This record has undergone validation or
            preliminary review. The reference sequence was derived from
            CP068256.2.
            
            Transcript Variant: This transcript contains two, common, single
            nucleotide deletions relative to the GRCh38 reference assembly.
            This transcript encodes a protein of 231 aa.
            
            ##RefSeq-Attributes-START##
            polymorphic pseudogene :: based on alignments, homology
            RefSeq Select criteria :: based on single protein-coding transcript
            ##RefSeq-Attributes-END##
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-696               CP068256.2         19404891-19405586
FEATURES             Location/Qualifiers
     source          1..696
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="22"
                     /map="22q11.21"
     gene            1..696
                     /gene="FAM246C"
                     /note="family with sequence similarity 246 member C
                     (gene/pseudogene)"
                     /db_xref="GeneID:117134596"
                     /db_xref="HGNC:HGNC:54842"
     CDS             1..696
                     /gene="FAM246C"
                     /codon_start=1
                     /product="protein FAM246C"
                     /protein_id="NP_001382956.1"
                     /db_xref="GeneID:117134596"
                     /db_xref="HGNC:HGNC:54842"
                     /translation="MAESGRPWAQARSAYRASEVLRRGTGRRRDPGPQSNGPGQEDAR
                     APGRMARLRGQLRAEAASRSEVPRLLKLVERAGAGAAGAGERTGAHSRGSVCSVCGEP
                     RGGATYPAGVLEVSERRLQEGLAAVREELGAGIEALRAELRAELDALRALLPPPPSPP
                     ARREPRAVPRAAPRGPTLPRTLGTVSALVAASRPADDAPDGPAECGAHRAPARKNHKK
                     MPVPPGAPQGGGD"
     exon            1..696
                     /gene="FAM246C"
                     /inference="alignment:Splign:2.1.0"
ORIGIN      
        1 atggcggagt ccggccgccc gtgggcccag gcgcgtagtg cgtacagagc cagcgaggtg
       61 ctgcggcgcg gcacgggccg ccggcgggat ccggggccgc aatccaatgg gccgggccag
      121 gaagacgccc gagccccggg ccggatggct cgcctgcgcg gccagctccg ggccgaagcg
      181 gcttcgcggt ccgaggtgcc gcggctgctg aagctggtgg agcgtgcggg ggccggggcg
      241 gcgggcgcgg gcgagaggac cggcgcgcac agccgcggct ccgtgtgctc ggtatgcggg
      301 gagccccgcg gcggggccac ctacccggcg ggggtcctgg aggtgagcga gcggcggctg
      361 caggagggcc tggcggcagt gcgcgaggag ctgggcgccg ggattgaggc gctgcgcgcg
      421 gagcttcgag cggagctgga tgccctgcgc gcgctgctgc cgccgccgcc gtccccgcct
      481 gcccgccgcg agccccgcgc cgtcccccgc gccgcgcccc gcggcccgac cctgccgcgg
      541 acgctcggca ccgtgagcgc cctggtcgcc gcctccaggc ccgcagacga cgccccggac
      601 ggcccagcag aatgcggagc gcaccgagcc ccggccagga agaaccacaa gaagatgcca
      661 gtgccgcctg gggccccgca aggtggcggg gactga
//
