Dbfetch
ID MN431453; SV 1; linear; genomic DNA; STD; HUM; 2978 BP. XX AC MN431453; XX DT 30-OCT-2020 (Rel. 144, Created) DT 11-MAR-2021 (Rel. 144, Last updated, Version 2) XX DE Homo sapiens clone C_112508_08375 MHC class I antigen (HLA-C) gene, DE complete cds. XX KW . XX OS Homo sapiens (human) OC Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; OC Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; OC Homo. XX RN [1] RP 1-2978 RA Cereb N., Yang S.Y.; RT "HLA new alleles found by Histogenetics"; RL Unpublished. XX RN [2] RP 1-2978 RA Cereb N., Yang S.Y.; RT ; RL Submitted (09-SEP-2019) to the INSDC. RL Histogenetics, 300 Executive Blvd, Ossining, NY 10562, USA XX DR MD5; ec43fa4e7d0e65a2b3d9cfee395cedd6. XX FH Key Location/Qualifiers FH FT source 1..2978 FT /organism="Homo sapiens" FT /mol_type="genomic DNA" FT /clone="C_112508_08375" FT /db_xref="taxon:9606" FT gene 1..2978 FT /gene="HLA-C" FT mRNA join(1..137,268..537,788..1063,1654..1929,2054..2173, FT 2614..2646,2754..2801,2966..2978) FT /gene="HLA-C" FT /product="MHC class I antigen" FT exon 1..137 FT /gene="HLA-C" FT /number=1 FT 5'UTR 1..64 FT /gene="HLA-C" FT CDS join(65..137,268..537,788..1063,1654..1929,2054..2173, FT 2614..2646,2754..2801,2966..2970) FT /codon_start=1 FT /gene="HLA-C" FT /product="MHC class I antigen" FT /protein_id="QFZ94675.1" FT /translation="MRVMAPRALLLLLSGGLALTETWACSHSMRYFDTAVSRPGRGEPR FT FISVGYVDDTQFVRFDSDAASPRGEPRAPWVEQEGPEYWDRETQKYKRQAQADRVSLRN FT LRGYYNQSEDGSHTLQRMSGCDLGPDGRLLRGYDQSAYDGKDYIALNEDLRSWTAADTA FT AQITQRKLEAARAAEQLRAYLEGTCVEWLRRYLENGKETLQRAEPPKTHVTHHPLSDHE FT ATLRCWALGFYPAEITLTWQRDGEDQTQDTELVETRPAGDGTFQKWAAVVVPSGQEQRY FT TCHMQHEGLQEPLTLSWEPSSQPTIPIMGIVAGLAVLVVLAVLGAVVTAMMCRRKSSGG FT KGGSCSQAACSNSAQGSDESLITCKA" FT intron 138..267 FT /gene="HLA-C" FT /number=1 FT exon 268..537 FT /gene="HLA-C" FT /number=2 FT intron 538..787 FT /gene="HLA-C" FT /number=2 FT exon 788..1063 FT /gene="HLA-C" FT /number=3 FT intron 1064..1653 FT /gene="HLA-C" FT /number=3 FT exon 1654..1929 FT /gene="HLA-C" FT /number=4 FT intron 1930..2053 FT /gene="HLA-C" FT /number=4 FT exon 2054..2173 FT /gene="HLA-C" FT /number=5 FT intron 2174..2613 FT /gene="HLA-C" FT /number=5 FT exon 2614..2646 FT /gene="HLA-C" FT /number=6 FT intron 2647..2753 FT /gene="HLA-C" FT /number=6 FT exon 2754..2801 FT /gene="HLA-C" FT /number=7 FT intron 2802..2965 FT /gene="HLA-C" FT /number=7 FT exon 2966..2978 FT /gene="HLA-C" FT /number=8 FT 3'UTR 2971..2978 FT /gene="HLA-C" XX SQ Sequence 2978 BP; 555 A; 878 C; 941 G; 604 T; 0 other; ccgcagtccc ggttctaaag tccccagtca cccacccgga ctcacattct ccccagaggc 60 cgagatgcgg gtcatggcgc cccgagccct cctcctgctg ctctcgggag gcctggccct 120 gaccgagacc tgggcctgtg agtgcggggt tgggagggaa gcggcctctg cggagaggag 180 cgaggggccc tcccggcgag ggcgcaggac ccggggagcc gcgcagggag gtgggtcggg 240 cgggtctcag cccctcctcg cccccaggct cccactccat gaggtatttc gacaccgccg 300 tgtcccggcc cggccgcgga gagccccgct tcatctcagt gggctacgtg gacgacacgc 360 agttcgtgcg gttcgacagc gacgccgcga gtccgagagg ggagccgcgg gcgccgtggg 420 tggagcagga ggggccggag tattgggacc gggagacaca gaagtacaag cgccaggcac 480 aggctgaccg agtgagcctg cggaacctgc gcggctacta caaccagagc gaggacggtg 540 agtgaccccg gcccggggcg caggtcacga cccctcccca tcccccacgg acggcccggg 600 tcgcccagag tctccccgtc tgagatccac cccaaggtgg atctgcggaa cccgcccaga 660 ccctcgaccg gagagagccc cagtcgcctt tacccggttt cattttcggt ttaggccaaa 720 atccccgcgg gttggtcggg gcggggcggg gctcggggga ctgggctgac cgcgggggcg 780 gggccagggt ctcacaccct ccagaggatg tctggctgcg acctggggcc cgacgggcgc 840 ctcctccgcg ggtatgacca gtccgcctac gacggcaagg attacatcgc cctgaacgag 900 gacctgcgct cctggaccgc cgcggacacc gcggctcaga tcacccagcg caagttggag 960 gcggcccgtg cggcggagca gctgagagcc tacctggagg gcacgtgcgt ggagtggctc 1020 cgcagatacc tggagaacgg gaaggagacg ctgcagcgcg caggtaccag gggcagtggg 1080 gagccttccc catctcctat agatctcccg ggatggcctc ccacgaggag gggaggaaaa 1140 tgggatcagc actggaatat cgccctccct tgaatggaga atggcatgag ttttcctgag 1200 tttcctcctc tgagggcccc ctctgctctc taggacaatt aagggatgaa gtctctgagg 1260 aaatggaggg gaagacagtc cctggaatac tgatcagggg tctcctttga ccactttgac 1320 cactgcagca gctgtggtca ggctgctgac ctttctctca ggccttgttc tctgcctcac 1380 actcaatgtg tctgaaggtt tgattccagc ttttctgagt cctgcagcct ccactcaggt 1440 caggaccaga agtcgctgtt cctccctcag agactagaac tttccaatga ataggagatt 1500 atcccaggtg cctgtgtcca ggctggcgtc tgggttctgt gccgccttcc ccaccccagg 1560 tgtcctgtcc attctcagga tggtcacatg ggcgctgctg gagtgtccca agagagatgc 1620 aaagtgtctg aattttctga ctcttcccgt cagaaccccc aaagacacac gtgacccacc 1680 accccctctc tgaccatgag gccaccctga ggtgctgggc cctgggcttc taccctgcgg 1740 agatcacact gacctggcag cgggatgggg aggaccagac ccaggacacc gagcttgtgg 1800 agaccaggcc agcaggagat ggaaccttcc agaagtgggc agctgtggtg gtgccttctg 1860 gacaagagca gagatacacg tgccatatgc agcacgaggg gctgcaagag cccctcaccc 1920 tgagctgggg taaggagggg aatggggggt cacatctctt atcagagaaa gcagaagtcc 1980 ttctggagcc cttcagccgg gtcagggctg aggcttgggg gtcagggccc ctcaccttct 2040 cctcctttcc cagagccatc ttcccagccc accatcccca tcatgggcat cgttgctggc 2100 ctggctgtcc tggttgtcct agctgtcctt ggagctgtgg tcaccgctat gatgtgtagg 2160 aggaagagct caggtaggga aggggtgaag agcggggtct gggttttctt gtcccactgg 2220 gagtttcaag ccccaggtag aagtgtgccc cgccttgtta ctggaagcac catccacaca 2280 tgggccatcc cagcctggga ccctgtgtgc cagcacttac tcttttgtga agcacatgtg 2340 acaatgaagg acggatgtat caccttgatg attatggtgt tggggtcctg attccagcat 2400 tcatgagtca ggggaaggtc cctgctaagg acagacctta ggagggcagt tggtccagaa 2460 cccacaactg ctttccccat gtttcctgat cctgccctgg gtctgcagtc gtagttctgg 2520 aaacttctct tgggtccaag actaggaggt tcccctaaga tcacatggcc ctgcctcctc 2580 ccagtcccct catagggcat tttcttccca caggtggaaa aggagggagc tgctctcagg 2640 ctgcgtgtaa gtgatggcgg cgggcgtgtg gaggagctca cctactccat aattcctctt 2700 gtcccacatc tcctgcgggc tctgaccagg tctttttttt tgttctaccc caggcagcaa 2760 cagtgcccag ggctctgatg agtctctcat cacttgtaaa ggtgagattc tggggagctg 2820 aagtggtcgg gggtggggca gagggaaaag gcctgggtaa tggggattct ttgattggga 2880 cgtttcgagt gtgtggtggg ccgttcagag tgtcatcgct taccatgact gacctgaatt 2940 tgttcatgac tattgtgttc tgtagcctga gacagctg 2978 //