Canonical Allele Identifier: CA2573333712
Gene: HLA-A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.[29942939C>G;29942940A>G;29942953T>A;29942965G>C;29942975G>C] , CM000668.2:g.[29942939C>G;29942940A>G;29942953T>A;29942965G>C;29942975G>C] GRCh38
NC_000006.11:g.[29910716C>G;29910717A>G;29910730T>A;29910742G>C;29910752G>C] , CM000668.1:g.[29910716C>G;29910717A>G;29910730T>A;29910742G>C;29910752G>C] GRCh37
NC_000006.10:g.[30018695C>G;30018696A>G;30018709T>A;30018721G>C;30018731G>C] NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000638375.2:c.[256C>G;257A>G;270T>A;282G>C;292G>C] ENSP00000492789.2:p.[Gln86Glu;Gln86Arg;Asn90Lys;Gln94His;Asp9...
ENST00000706892.1:n.[532C>G;533A>G;546T>A;558G>C;568G>C]
ENST00000706893.1:c.[256C>G;257A>G;270T>A;282G>C;292G>C] ENSP00000516609.1:p.[Gln86Glu;Gln86Arg;Asn90Lys;Gln94His;Asp9...
ENST00000706894.1:c.[256C>G;257A>G;270T>A;282G>C;292G>C] ENSP00000516610.1:p.[Gln86Glu;Gln86Arg;Asn90Lys;Gln94His;Asp9...
ENST00000706895.1:n.[532C>G;533A>G;546T>A;558G>C;568G>C]
ENST00000706896.1:n.[532C>G;533A>G;546T>A;558G>C;568G>C]
ENST00000706897.1:n.[532C>G;533A>G;546T>A;558G>C;568G>C]
ENST00000706898.1:c.[256C>G;257A>G;270T>A;282G>C;292G>C] ENSP00000516611.1:p.[Gln86Glu;Gln86Arg;Asn90Lys;Gln94His;Asp9...
ENST00000706899.1:n.[532C>G;533A>G;546T>A;558G>C;568G>C]
ENST00000706900.1:c.[172C>G;173A>G;186T>A;198G>C;208G>C] ENSP00000516617.1:p.[Gln58Gly;Asn62Lys;Gln66His;Asp70His]
ENST00000706901.1:c.[256C>G;257A>G;270T>A;282G>C;292G>C] ENSP00000516612.1:p.[Gln86Glu;Gln86Arg;Asn90Lys;Gln94His;Asp9...
ENST00000706902.1:c.[256C>G;257A>G;270T>A;282G>C;292G>C] ENSP00000516613.1:p.[Gln86Glu;Gln86Arg;Asn90Lys;Gln94His;Asp9...
ENST00000706903.1:c.[256C>G;257A>G;270T>A;282G>C;292G>C] ENSP00000516614.1:p.[Gln86Glu;Gln86Arg;Asn90Lys;Gln94His;Asp9...
ENST00000706904.1:c.[256C>G;257A>G;270T>A;282G>C;292G>C] ENSP00000516615.1:p.[Gln86Glu;Gln86Arg;Asn90Lys;Gln94His;Asp9...
ENST00000706905.1:c.[256C>G;257A>G;270T>A;282G>C;292G>C] ENSP00000516616.1:p.[Gln86Gly;Asn90Lys;Gln94His;Asp98His]
ENST00000376809.10:c.[256C>G;257A>G;270T>A;282G>C;292G>C] MANE Select ENSP00000366005.5:p.[Gln86Gly;Asn90Lys;Gln94His;Asp98His]
ENST00000638375.1:c.[256C>G;257A>G;270T>A;282G>C;292G>C] ENSP00000492789.1:p.[Gln86Glu;Gln86Arg;Asn90Lys;Gln94His;Asp9...
ENST00000376802.2:c.[256C>G;257A>G;270T>A;282G>C;292G>C] ENSP00000365998.2:p.[Gln86Gly;Asn90Lys;Gln94His;Asp98His]
ENST00000376806.9:c.[256C>G;257A>G;270T>A;282G>C;292G>C] ENSP00000366002.5:p.[Gln86Glu;Gln86Arg;Asn90Lys;Gln94His;Asp9...
ENST00000376809.9:c.[256C>G;257A>G;270T>A;282G>C;292G>C] ENSP00000366005.5:p.[Gln86Glu;Gln86Arg;Asn90Lys;Gln94His;Asp9...
ENST00000396634.5:c.[256C>G;257A>G;270T>A;282G>C;292G>C] ENSP00000379873.1:p.[Gln86Gly;Asn90Lys;Gln94His;Asp98His]
ENST00000429656.1:n.[93C>G;103C>G;115A>T;128T>C;129G>C]
ENST00000461903.1:n.[256C>G;257A>G;270T>A;282G>C;292G>C]
ENST00000479320.5:n.[256C>G;257A>G;270T>A;282G>C;292G>C]
ENST00000495183.5:n.[258C>G;259A>G;272T>A;284G>C;294G>C]
ENST00000496081.5:n.[177+85C>G;177+86A>G;177+99T>A;177+111G>C;177+121G>C]
NM_002116.7:c.[256C>G;257A>G;270T>A;282G>C;292G>C] NP_002107.3:p.[Gln86Glu;Gln86Arg;Asn90Lys;Gln94His;Asp98His]
NM_002116.8:c.[256C>G;257A>G;270T>A;282G>C;292G>C] MANE Select NP_002107.3:p.[Gln86Gly;Asn90Lys;Gln94His;Asp98His]