Canonical Allele Identifier: CA2573333708
Gene: HLA-A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.[29942923G>T;29942939C>G;29942940A>G;29942953T>A] , CM000668.2:g.[29942923G>T;29942939C>G;29942940A>G;29942953T>A] GRCh38
NC_000006.11:g.[29910700G>T;29910716C>G;29910717A>G;29910730T>A] , CM000668.1:g.[29910700G>T;29910716C>G;29910717A>G;29910730T>A] GRCh37
NC_000006.10:g.[30018679G>T;30018695C>G;30018696A>G;30018709T>A] NCBI36
NG_029217.2:g.[5458G>T;5474C>G;5475A>G;5488T>A]

Transcript Alleles

HGVS Amino-acid Change
ENST00000638375.2:c.[240G>T;256C>G;257A>G;270T>A] ENSP00000492789.2:p.[Gly80=;Gln86Glu;Gln86Arg;Asn90Lys]
ENST00000706892.1:n.[516G>T;532C>G;533A>G;546T>A]
ENST00000706893.1:c.[240G>T;256C>G;257A>G;270T>A] ENSP00000516609.1:p.[Gly80=;Gln86Glu;Gln86Arg;Asn90Lys]
ENST00000706894.1:c.[240G>T;256C>G;257A>G;270T>A] ENSP00000516610.1:p.[Gly80=;Gln86Glu;Gln86Arg;Asn90Lys]
ENST00000706895.1:n.[516G>T;532C>G;533A>G;546T>A]
ENST00000706896.1:n.[516G>T;532C>G;533A>G;546T>A]
ENST00000706897.1:n.[516G>T;532C>G;533A>G;546T>A]
ENST00000706898.1:c.[240G>T;256C>G;257A>G;270T>A] ENSP00000516611.1:p.[Gly80=;Gln86Glu;Gln86Arg;Asn90Lys]
ENST00000706899.1:n.[516G>T;532C>G;533A>G;546T>A]
ENST00000706900.1:c.[156G>T;172C>G;173A>G;186T>A] ENSP00000516617.1:p.[Gly52=;Gln58Gly;Asn62Lys]
ENST00000706901.1:c.[240G>T;256C>G;257A>G;270T>A] ENSP00000516612.1:p.[Gly80=;Gln86Glu;Gln86Arg;Asn90Lys]
ENST00000706902.1:c.[240G>T;256C>G;257A>G;270T>A] ENSP00000516613.1:p.[Gly80=;Gln86Glu;Gln86Arg;Asn90Lys]
ENST00000706903.1:c.[240G>T;256C>G;257A>G;270T>A] ENSP00000516614.1:p.[Gly80=;Gln86Glu;Gln86Arg;Asn90Lys]
ENST00000706904.1:c.[240G>T;256C>G;257A>G;270T>A] ENSP00000516615.1:p.[Gly80=;Gln86Glu;Gln86Arg;Asn90Lys]
ENST00000706905.1:c.[240G>T;256C>G;257A>G;270T>A] ENSP00000516616.1:p.[Gly80=;Gln86Gly;Asn90Lys]
ENST00000376809.10:c.[240G>T;256C>G;257A>G;270T>A] MANE Select ENSP00000366005.5:p.[Gly80=;Gln86Gly;Asn90Lys]
ENST00000638375.1:c.[240G>T;256C>G;257A>G;270T>A] ENSP00000492789.1:p.[Gly80=;Gln86Glu;Gln86Arg;Asn90Lys]
ENST00000376802.2:c.[240G>T;256C>G;257A>G;270T>A] ENSP00000365998.2:p.[Gly80=;Gln86Gly;Asn90Lys]
ENST00000376806.9:c.[240G>T;256C>G;257A>G;270T>A] ENSP00000366002.5:p.[Gly80=;Gln86Glu;Gln86Arg;Asn90Lys]
ENST00000376809.9:c.[240G>T;256C>G;257A>G;270T>A] ENSP00000366005.5:p.[Gly80=;Gln86Glu;Gln86Arg;Asn90Lys]
ENST00000396634.5:c.[240G>T;256C>G;257A>G;270T>A] ENSP00000379873.1:p.[Gly80=;Gln86Gly;Asn90Lys]
ENST00000429656.1:n.[115A>T;128T>C;129G>C;145C>A]
ENST00000461903.1:n.[240G>T;256C>G;257A>G;270T>A]
ENST00000479320.5:n.[240G>T;256C>G;257A>G;270T>A]
ENST00000495183.5:n.[242G>T;258C>G;259A>G;272T>A]
ENST00000496081.5:n.[177+69G>T;177+85C>G;177+86A>G;177+99T>A]
NM_002116.7:c.[240G>T;256C>G;257A>G;270T>A] NP_002107.3:p.[Gly80=;Gln86Glu;Gln86Arg;Asn90Lys]
NM_002116.8:c.[240G>T;256C>G;257A>G;270T>A] MANE Select NP_002107.3:p.[Gly80=;Gln86Gly;Asn90Lys]
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