Dbfetch
ID KF114897; SV 1; linear; genomic DNA; STD; HUM; 1022 BP. XX AC KF114897; XX DT 15-SEP-2013 (Rel. 118, Created) DT 15-SEP-2013 (Rel. 118, Last updated, Version 1) XX DE Homo sapiens MHC class I antigen (HLA-C) gene, HLA-C*16:01 variant allele, DE exons 2 through 4 and partial 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 1-1022 RA Hodges E., Young C., Chen D.; RT ; RL Submitted (20-MAY-2013) to the INSDC. RL Clinical Transplantation Immunology Laboratory, Duke University Medical RL Center, DUMC 3712, Research Park 3, Room 116, Durham, NC 27710, USA XX DR MD5; bafbff14744aef184e64a2a8256af599. DR IMGT/HLA; HLA-C*16:39:02; HLA09822. XX CC ##Assembly-Data-START## CC Sequencing Technology :: Sanger dideoxy sequencing CC ##Assembly-Data-END## XX FH Key Location/Qualifiers FH FT source 1..1022 FT /organism="Homo sapiens" FT /mol_type="genomic DNA" FT /db_xref="taxon:9606" FT gene <1..>1022 FT /gene="HLA-C" FT /allele="HLA-C*16:01 variant" FT mRNA join(<1..270,371..646,747..>1022) FT /gene="HLA-C" FT /allele="HLA-C*16:01 variant" FT /product="MHC class I antigen" FT CDS join(<1..270,371..646,747..>1022) FT /codon_start=3 FT /gene="HLA-C" FT /allele="HLA-C*16:01 variant" FT /product="MHC class I antigen" FT /db_xref="InterPro:IPR001039" FT /db_xref="InterPro:IPR003006" FT /db_xref="InterPro:IPR003597" FT /db_xref="InterPro:IPR007110" FT /db_xref="InterPro:IPR011161" FT /db_xref="InterPro:IPR011162" FT /db_xref="InterPro:IPR013783" FT /db_xref="InterPro:IPR036179" FT /db_xref="InterPro:IPR037055" FT /db_xref="UniProtKB/TrEMBL:T2B9H9" FT /protein_id="AGV08317.1" FT /translation="SHSMRYFYTAVSRPGRREPRFIAVGYVDDTQFVRFDSDAASPRGE FT PRAPWVEQEGPEYWDRETQKYKRQAQTDRVSLRNLRGYYNQSEAGSHTLQWMYGCDLGP FT DGRLLRGYDQSAYDGKDYIALNEDLRSWTAADTAAQITQRKWEAARAAEQQRAYLEGTC FT VEWLRRYLENGKETLQRAEHPKTHVTHHLVSDHEATLRCWALGFYPAEITLTWQRDGED FT QTQDTELVETRPAGDGTFQKWAAVVVPSGEEQRYTCHVQHEGLPEPLTLRW" FT exon 1..270 FT /gene="HLA-C" FT /allele="HLA-C*16:01 variant" FT /number=2 FT gap 271..370 FT /estimated_length=unknown FT exon 371..646 FT /gene="HLA-C" FT /allele="HLA-C*16:01 variant" FT /number=3 FT gap 647..746 FT /estimated_length=unknown FT exon 747..1022 FT /gene="HLA-C" FT /allele="HLA-C*16:01 variant" FT /number=4 XX SQ Sequence 1022 BP; 170 A; 255 C; 286 G; 111 T; 200 other; gctcccactc catgaggtat ttctacaccg ccgtgtcccg gcccggccgc agagagcccc 60 gcttcatcgc agtgggctac gtggacgaca cgcagttcgt gcggttcgac agcgacgccg 120 cgagtccaag aggggagccg cgggcgccgt gggtggagca ggaggggccg gagtattggg 180 accgggagac acagaagtac aagcgccagg cacagactga ccgagtgagc ctgcggaacc 240 tgcgcggcta ctacaaccag agcgaggccg nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 300 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 360 nnnnnnnnnn ggtctcacac cctccagtgg atgtatggct gcgacctggg gcccgacggg 420 cgcctcctcc gcgggtatga ccagtccgcc tacgacggca aggattacat cgccctgaac 480 gaggacctgc gctcctggac cgccgcggac acggcggctc agatcaccca gcgcaagtgg 540 gaggcggccc gtgcggcgga gcagcagaga gcctacctgg agggcacgtg cgtggagtgg 600 ctccgcagat acctggagaa cgggaaggag acgctgcagc gcgcggnnnn nnnnnnnnnn 660 nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 720 nnnnnnnnnn nnnnnnnnnn nnnnnnaaca cccaaagaca cacgtgaccc accatctcgt 780 ctctgaccat gaggccaccc tgaggtgctg ggccctgggc ttctaccctg cggagatcac 840 actgacctgg cagcgggatg gcgaggacca aactcaggac accgagcttg tggagaccag 900 gccagcagga gatggaacct tccagaagtg ggcagctgtg gtggtgcctt ctggagaaga 960 gcagagatac acgtgccatg tgcagcacga ggggctgccg gagcccctca ccctgagatg 1020 gg 1022 //