Canonical Allele Identifier: CA2573333707
Gene: HLA-A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.[29942923G>T;29942939C>G;29942940A>G;29942953T>A;29942965G>C;29942975G>C;29943451A>T;29943462T>C;29943463T>A] , CM000668.2:g.[29942923G>T;29942939C>G;29942940A>G;29942953T>A;29942965G>C;29942975G>C;29943451A>T;29943462T>C;29943463T>A] GRCh38
NC_000006.11:g.[29910700G>T;29910716C>G;29910717A>G;29910730T>A;29910742G>C;29910752G>C;29911228A>T;29911239T>C;29911240T>A] , CM000668.1:g.[29910700G>T;29910716C>G;29910717A>G;29910730T>A;29910742G>C;29910752G>C;29911228A>T;29911239T>C;29911240T>A] GRCh37
NC_000006.10:g.[30018679G>T;30018695C>G;30018696A>G;30018709T>A;30018721G>C;30018731G>C;30019207A>T;30019218T>C;30019219T>A] NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000638375.2:c.[240G>T;256C>G;257A>G;270T>A;282G>C;292G>C;527A>T;538T>C;539T>A] ENSP00000492789.2:p.[Gly80=;Gln86Glu;Gln86Arg;Asn90Lys;Gln94H...
ENST00000706892.1:n.[516G>T;532C>G;533A>G;546T>A;558G>C;568G>C;803A>T;814T>C;815T>A]
ENST00000706893.1:c.[240G>T;256C>G;257A>G;270T>A;282G>C;292G>C;527A>T;538T>C;539T>A] ENSP00000516609.1:p.[Gly80=;Gln86Glu;Gln86Arg;Asn90Lys;Gln94H...
ENST00000706894.1:c.[240G>T;256C>G;257A>G;270T>A;282G>C;292G>C;527A>T;538T>C;539T>A] ENSP00000516610.1:p.[Gly80=;Gln86Glu;Gln86Arg;Asn90Lys;Gln94H...
ENST00000706895.1:n.[516G>T;532C>G;533A>G;546T>A;558G>C;568G>C;803A>T;814T>C;815T>A]
ENST00000706896.1:n.[516G>T;532C>G;533A>G;546T>A;558G>C;568G>C;803A>T;814T>C;815T>A]
ENST00000706897.1:n.[516G>T;532C>G;533A>G;546T>A;558G>C;568G>C;803A>T;814T>C;815T>A]
ENST00000706898.1:c.[240G>T;256C>G;257A>G;270T>A;282G>C;292G>C;527A>T;538T>C;539T>A] ENSP00000516611.1:p.[Gly80=;Gln86Glu;Gln86Arg;Asn90Lys;Gln94H...
ENST00000706899.1:n.[516G>T;532C>G;533A>G;546T>A;558G>C;568G>C;803A>T;814T>C;815T>A]
ENST00000706900.1:c.[156G>T;172C>G;173A>G;186T>A;198G>C;208G>C;443A>T;454T>C;455T>A] ENSP00000516617.1:p.[Gly52=;Gln58Gly;Asn62Lys;Gln66His;Asp70H...
ENST00000706901.1:c.[240G>T;256C>G;257A>G;270T>A;282G>C;292G>C;527A>T;538T>C;539T>A] ENSP00000516612.1:p.[Gly80=;Gln86Glu;Gln86Arg;Asn90Lys;Gln94H...
ENST00000706902.1:c.[240G>T;256C>G;257A>G;270T>A;282G>C;292G>C;527A>T;538T>C;539T>A] ENSP00000516613.1:p.[Gly80=;Gln86Glu;Gln86Arg;Asn90Lys;Gln94H...
ENST00000706903.1:c.[240G>T;256C>G;257A>G;270T>A;282G>C;292G>C;527A>T;538T>C;539T>A] ENSP00000516614.1:p.[Gly80=;Gln86Glu;Gln86Arg;Asn90Lys;Gln94H...
ENST00000706904.1:c.[240G>T;256C>G;257A>G;270T>A;282G>C;292G>C;527A>T;538T>C;539T>A] ENSP00000516615.1:p.[Gly80=;Gln86Glu;Gln86Arg;Asn90Lys;Gln94H...
ENST00000706905.1:c.[240G>T;256C>G;257A>G;270T>A;282G>C;292G>C;527A>T;538T>C;539T>A] ENSP00000516616.1:p.[Gly80=;Gln86Gly;Asn90Lys;Gln94His;Asp98H...
ENST00000376809.10:c.[240G>T;256C>G;257A>G;270T>A;282G>C;292G>C;527A>T;538T>C;539T>A] MANE Select ENSP00000366005.5:p.[Gly80=;Gln86Gly;Asn90Lys;Gln94His;Asp98H...
ENST00000638375.1:c.[240G>T;256C>G;257A>G;270T>A;282G>C;292G>C;527A>T;538T>C;539T>A] ENSP00000492789.1:p.[Gly80=;Gln86Glu;Gln86Arg;Asn90Lys;Gln94H...
ENST00000376802.2:c.[240G>T;256C>G;257A>G;270T>A;282G>C;292G>C;527A>T;538T>C;539T>A] ENSP00000365998.2:p.[Gly80=;Gln86Gly;Asn90Lys;Gln94His;Asp98H...
ENST00000376806.9:c.[240G>T;256C>G;257A>G;270T>A;282G>C;292G>C;527A>T;538T>C;539T>A] ENSP00000366002.5:p.[Gly80=;Gln86Glu;Gln86Arg;Asn90Lys;Gln94H...
ENST00000376809.9:c.[240G>T;256C>G;257A>G;270T>A;282G>C;292G>C;527A>T;538T>C;539T>A] ENSP00000366005.5:p.[Gly80=;Gln86Glu;Gln86Arg;Asn90Lys;Gln94H...
ENST00000396634.5:c.[240G>T;256C>G;257A>G;270T>A;282G>C;292G>C;527A>T;538T>C;539T>A] ENSP00000379873.1:p.[Gly80=;Gln86Gly;Asn90Lys;Gln94His;Asp98H...
ENST00000461903.1:n.[240G>T;256C>G;257A>G;270T>A;282G>C;292G>C;768A>T;779T>C;780T>A]
ENST00000479320.5:n.[240G>T;256C>G;257A>G;270T>A;282G>C;292G>C;768A>T;779T>C;780T>A]
ENST00000495183.5:n.[242G>T;258C>G;259A>G;272T>A;284G>C;294G>C;770A>T;781T>C;782T>A]
ENST00000496081.5:n.[177+69G>T;177+85C>G;177+86A>G;177+99T>A;177+111G>C;177+121G>C;344A>T;355T>C;356T>A]
NM_002116.7:c.[240G>T;256C>G;257A>G;270T>A;282G>C;292G>C;527A>T;538T>C;539T>A] NP_002107.3:p.[Gly80=;Gln86Glu;Gln86Arg;Asn90Lys;Gln94His;Asp...
NM_002116.8:c.[240G>T;256C>G;257A>G;270T>A;282G>C;292G>C;527A>T;538T>C;539T>A] MANE Select NP_002107.3:p.[Gly80=;Gln86Gly;Asn90Lys;Gln94His;Asp98His;Glu...