Dbfetch
ID OM066773; SV 1; linear; genomic DNA; STD; HUM; 2864 BP. XX AC OM066773; XX DT 04-DEC-2022 (Rel. 144, Created) DT 05-DEC-2022 (Rel. 144, Last updated, Version 1) XX DE Homo sapiens MHC class I antigen (HLA-G) gene, HLA-G*01:01:01:01v2var DE allele, 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 1-2864 RA Enrich E.; RT ; RL Submitted (15-DEC-2021) to the INSDC. RL Histocompatibility and Immunogenetics Laboratory, Blood and Tissue Bank, RL Passeig Taulat 116, Barcelona, Barcelona 08005, Spain XX DR MD5; 12d4809f46681504b77e575ad406ce73. XX CC ##Assembly-Data-START## CC Assembly Method :: NGSengine v. 2.22.0.22581 CC Sequencing Technology :: Illumina CC ##Assembly-Data-END## XX FH Key Location/Qualifiers FH FT source 1..2864 FT /organism="Homo sapiens" FT /mol_type="genomic DNA" FT /country="Spain" FT /db_xref="taxon:9606" FT gene <1..>2864 FT /gene="HLA-G" FT /allele="HLA-G*01:01:01:01v2var" FT mRNA join(<1..99,229..498,725..1000,1600..1875,1998..2114, FT 2560..>2864) FT /gene="HLA-G" FT /allele="HLA-G*01:01:01:01v2var" FT /product="MHC class I antigen" FT exon <1..99 FT /gene="HLA-G" FT /allele="HLA-G*01:01:01:01v2var" FT /number=1 FT 5'UTR <1..26 FT /gene="HLA-G" FT /allele="HLA-G*01:01:01:01v2var" FT CDS join(27..99,229..498,725..1000,1600..1875,1998..2114, FT 2560..2564) FT /codon_start=1 FT /gene="HLA-G" FT /allele="HLA-G*01:01:01:01v2var" FT /product="MHC class I antigen" FT /protein_id="UZY20097.1" FT /translation="MVVMAPRTLFLLLSGALTLTETWAGSHSMRYFSAAVSRPGRGEPR FT FIAMGYVDDTQFVRFDSDSACPRMEPRAPWVEQEGPEYWEEETRNTKAHAQTDRMNLQT FT LRGYYNQSEASSHTLQWMIGCDLGSDGRLLRGYEQYAYDGKDYLALNEDLRSWTAADTA FT AQISKRKCEAANVAEQRRAYLEGTCVEWLHRYLENGKEMLQRADPPKTHVTHHPVFDYE FT ATLRCWALGFYPAEIILTWQRDGEDQTQDVELVETRPAGDGTFQKWAAVVVPSGEEQRY FT TCHVQHEGLPEPLMLRWKQSSLPTIPIMGIVAGLVVLAAVVTGAAVAAVLWRKKSSD" FT exon 229..498 FT /gene="HLA-G" FT /allele="HLA-G*01:01:01:01v2var" FT /number=2 FT exon 725..1000 FT /gene="HLA-G" FT /allele="HLA-G*01:01:01:01v2var" FT /number=3 FT exon 1600..1875 FT /gene="HLA-G" FT /allele="HLA-G*01:01:01:01v2var" FT /number=4 FT exon 1998..2114 FT /gene="HLA-G" FT /allele="HLA-G*01:01:01:01v2var" FT /number=5 FT exon 2560..>2864 FT /gene="HLA-G" FT /allele="HLA-G*01:01:01:01v2var" FT /number=6 FT 3'UTR 2565..>2864 FT /gene="HLA-G" FT /allele="HLA-G*01:01:01:01v2var" XX SQ Sequence 2864 BP; 554 A; 827 C; 902 G; 581 T; 0 other; ggactcattc tccccagacg ccaaggatgg tggtcatggc gccccgaacc ctcttcctgc 60 tgctctcggg ggccctgacc ctgaccgaga cctgggcggg tgagtgcggg gtcaggaggg 120 aaacggcccc tgcgcggagg agggaggggc ccgcctggcg ggggcgcagg actcggcagc 180 cgcgccggga ggagggtcgg gcgggtctca acccctcctc gcccccaggc tcccactcca 240 tgaggtattt cagcgccgcc gtgtcccggc ccggccgcgg ggagccccgc ttcatcgcca 300 tgggctacgt ggacgacacg cagttcgtgc ggttcgacag cgactcggcg tgtccgagga 360 tggagccgcg ggcgccgtgg gtggagcagg aggggccgga gtattgggaa gaggagacac 420 ggaacaccaa ggcccacgca cagactgaca gaatgaacct gcagaccctg cgcggctact 480 acaaccagag cgaggccagt gagtaactcc ggcccaggga gcagatcacg acccccacct 540 ccatgcccca cggacggccc gggtactccc gagtctccgg gtctgggatc caccccgagg 600 ccgcgggacc cgcccagacc ctctacctgg gagaacccca aggcgccttt accaaaatcc 660 ccgcgggtgg gtccgggcga gggcgaggct cggtgggcgg ggctgaccga gggggtgggg 720 ccaggttctc acaccctcca gtggatgatt ggctgcgacc tggggtccga cggacgcctc 780 ctccgcgggt atgaacagta tgcctacgat ggcaaggatt acctcgccct gaacgaggac 840 ctgcgctcct ggaccgcagc ggacactgcg gctcagatct ccaagcgcaa gtgtgaggcg 900 gccaatgtgg ctgaacaaag gagagcctac ctggagggca cgtgcgtgga gtggctccac 960 agatacctgg agaacgggaa ggagatgctg cagcgcgcgg gtaccagggg cagtggggcg 1020 cctccctgat ctcctgtaga cctctcagcc tggcctagca caaggagagg aggaaaatgg 1080 gaccaacact agaatatcgc cctccctctg gtcctgaggg agaggaatcc tcctgggttt 1140 ccagatcctg taccagagag tgattctgag ggcccgtcct gctctctggg acaattaagg 1200 gatgaagtct ctgagggagt ggaggggaag acaatccctg gaagactgat caggggttcc 1260 ctttgacccc acagcagcct tggcaccagg acttttcccc tcaggccttg ttctctgcct 1320 cacactcaat gtgtgtgggg gtctgactcc agctcctctg agtcccttgg cctccactca 1380 ggtcagaacc ggaggtccct gctcccccgc tcagagacta gaactttcca aggaatagga 1440 gattatccca ggtgcccgtg tccaggctgg tgtctgggtt ctgtgctccc ttccccaccc 1500 caggtatctg gttcattctt aggatggtca catccaggtg ctgctggagt gtcccatgag 1560 agatgcaaag tgcttgaatt ttctgactct tcctttcaga cccccccaag acacacgtga 1620 cccaccaccc tgtctttgac tatgaggcca ccctgaggtg ctgggccctg ggcttctacc 1680 ctgcggagat catactgacc tggcagcggg atggggagga ccagacccag gacgtggagc 1740 tcgtggagac caggcctgca ggggatggaa ccttccagaa gtgggcagct gtggtggtgc 1800 cttctggaga ggagcagaga tacacgtgcc atgtgcagca tgaggggctg ccggagcccc 1860 tcatgctgag atggagtaag gagggagatg gaggcatcat gtctgttagg gaaagcagga 1920 gcctctctga agacctttaa cagggtcggt ggtgagggct gggggtcaga gaccctcacc 1980 ttcacctcct ttcccagagc agtcttccct gcccaccatc cccatcatgg gtatcgttgc 2040 tggcctggtt gtccttgcag ctgtagtcac tggagctgca gtcgctgctg tgctgtggag 2100 aaagaagagc tcaggtaagg aaggggtgac aagtggggtc tgagttttct tgtcccactg 2160 ggggtttcaa gccccaggta gaagtgtgcc ctgcctggtt actgggaagc accatccaca 2220 ctcatgggcc tacccagcct gggccctgtg tgccagcacc ttctcttttg taaagcacct 2280 gtgacaatga aggacagatt tattaccttg atgattgtag tgatggggac ctgatcccag 2340 taatcacagg tcaggagaag gtccctggct aaggacagac cttaggaggg cagttggtcg 2400 aggacccaca tctgctttcc ttgtttttcc tgatcccgcc ctgggtctgc agtcacacat 2460 ttctggaaac ttctcgaggg tccaagacta ggaggttcct ctaggacctc atggccctgc 2520 cacctttctg gcctctcaca ggacattttc ttcccacaga ttgaaaagga gggagctact 2580 ctcaggctgc aagtaagtat gaaggaggct gatccctgag atccttggga tcttgtgttt 2640 gggagcccat gggggagctc acccacccca caattcctcc tctggccaca tctcctgtgg 2700 tctctgacca ggtgctgttt ttgttctact ctaggcagtg acagtgccca gggctctaat 2760 gtgtctctca cggcttgtaa atgtgacacc ccggggggcc tgatgtgtgt gggttgttga 2820 ggggaacagg ggacatagct gtgctatgag gtttctttga cttc 2864 //