LOCUS       HUMCACH2D                882 bp    mRNA    linear   HUM 06-MAR-1995
DEFINITION  Human cardiac L-type calcium channel (CCHL1A1) mRNA, partial cds.
ACCESSION   M57971 J05675
VERSION     M57971.1
KEYWORDS    cardiac L-type calcium channel alpha-1.
SOURCE      Homo sapiens (human)
  ORGANISM  Homo sapiens
            Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
            Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini;
            Catarrhini; Hominidae; Homo.
REFERENCE   1  (bases 1 to 882)
  AUTHORS   Perez-Reyes,E., Wei,X.Y., Castellano,A. and Birnbaumer,L.
  TITLE     Molecular diversity of L-type calcium channels. Evidence for
            alternative splicing of the transcripts of three non-allelic genes
  JOURNAL   J. Biol. Chem. 265 (33), 20430-20436 (1990)
   PUBMED   2173707
COMMENT     Original source text: Homo sapiens (clone HUM421) male heart cDNA
            to mRNA.
FEATURES             Location/Qualifiers
     source          1..882
                     /db_xref="H-InvDB:HIT000195854"
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /map="12pter-p12"
                     /clone="HUM421"
                     /sex="male"
                     /tissue_type="heart"
     gene            1..882
                     /gene="CCHL1A1"
     CDS             <1..>882
                     /gene="CCHL1A1"
                     /standard_name="Cach2d"
                     /note="region from bp 346-462 differs other clones (e.g.
                     hum 428); splice variant"
                     /codon_start=1
                     /product="L-type calcium channel alpha-1"
                     /protein_id="AAA62832.1"
                     /translation="VGFVIVTFQEQGEQEYKNCELDKNQRQCVEYALKARPLRRYIPK
                     NQHQYKVWYVVNSTYFEYLMFVLILLNTICLAMQHYGQSCLFKIAMNILNMLFTGLFT
                     VEMILKLIAFKPKHYFCDAWNTFDALIVVGSIVDIAITEVNPAEHTQCSPSMNAEENS
                     RISITFFRLFRVMRLVKLLSRGEGIRTLLWTFIKSFQALPYVALLIVMLFFIYAVIGM
                     QVFGKIALNDTTEINRNNNFQTFPQAVLLLFRCATGEAWQDIMLACMPGKKCAPESEP
                     SNSTEGETPCGSSFAVFY"
     misc_difference 430..462
                     /gene="CCHL1A1"
                     /note="variants contain a deletion of 33 nucleotides at
                     position 430; splice variant"
BASE COUNT          197 a          263 c          224 g          198 t
ORIGIN      
        1 gtgggcttcg tcatcgtcac ctttcaggag cagggggagc aggagtacaa gaactgtgag
       61 ctggacaaga accagcgaca gtgcgtggaa tacgccctca aggcccggcc cctgcggagg
      121 tacatcccca agaaccagca ccagtacaaa gtgtggtacg tggtcaactc cacctacttc
      181 gagtacctga tgttcgtcct catcctgctc aacaccatct gcctggccat gcagcactac
      241 ggccagagct gcctgttcaa aatcgccatg aacatcctca acatgctctt cactggcctc
      301 ttcaccgtgg agatgatcct gaagctcatt gccttcaaac ccaagcacta tttctgtgat
      361 gcatggaata catttgacgc cttgattgtt gtgggtagca ttgttgatat agcaatcacc
      421 gaggtaaacc cagctgaaca tacccaatgc tctccctcta tgaacgcaga ggaaaactcc
      481 cgcatctcca tcaccttctt ccgcctgttc cgggtcatgc gtctggtgaa gctgctgagc
      541 cgtggggagg gcatccggac gctgctgtgg accttcatca agtccttcca ggccctgccc
      601 tatgtggccc tcctgatcgt gatgctgttc ttcatctacg cggtgatcgg gatgcaggtg
      661 tttgggaaaa ttgccctgaa tgataccaca gagatcaacc ggaacaacaa ctttcagacc
      721 ttcccccagg ccgtgctgct cctcttcagg tgtgccaccg gggaggcctg gcaggacatc
      781 atgctggcct gcatgccagg caagaagtgt gccccagagt ccgagcccag caacagcacg
      841 gagggtgaaa caccctgtgg tagcagcttt gctgtcttct ac
//