Canonical Allele Identifier: CA2573333718
Gene: HLA-A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.[29942939C>G;29942948C>G;29942953T>A] , CM000668.2:g.[29942939C>G;29942948C>G;29942953T>A] GRCh38
NC_000006.11:g.[29910716C>G;29910725C>G;29910730T>A] , CM000668.1:g.[29910716C>G;29910725C>G;29910730T>A] GRCh37
NC_000006.10:g.[30018695C>G;30018704C>G;30018709T>A] NCBI36
NG_029217.2:g.[5474C>G;5483C>G;5488T>A]

Transcript Alleles

HGVS Amino-acid Change
ENST00000638375.2:c.[256C>G;265C>G;270T>A] ENSP00000492789.2:p.[Gln86Glu;Arg89Gly;Asn90Lys]
ENST00000706892.1:n.[532C>G;541C>G;546T>A]
ENST00000706893.1:c.[256C>G;265C>G;270T>A] ENSP00000516609.1:p.[Gln86Glu;Arg89Gly;Asn90Lys]
ENST00000706894.1:c.[256C>G;265C>G;270T>A] ENSP00000516610.1:p.[Gln86Glu;Arg89Gly;Asn90Lys]
ENST00000706895.1:n.[532C>G;541C>G;546T>A]
ENST00000706896.1:n.[532C>G;541C>G;546T>A]
ENST00000706897.1:n.[532C>G;541C>G;546T>A]
ENST00000706898.1:c.[256C>G;265C>G;270T>A] ENSP00000516611.1:p.[Gln86Glu;Arg89Gly;Asn90Lys]
ENST00000706899.1:n.[532C>G;541C>G;546T>A]
ENST00000706900.1:c.[172C>G;181C>G;186T>A] ENSP00000516617.1:p.[Gln58Glu;Arg61Gly;Asn62Lys]
ENST00000706901.1:c.[256C>G;265C>G;270T>A] ENSP00000516612.1:p.[Gln86Glu;Arg89Gly;Asn90Lys]
ENST00000706902.1:c.[256C>G;265C>G;270T>A] ENSP00000516613.1:p.[Gln86Glu;Arg89Gly;Asn90Lys]
ENST00000706903.1:c.[256C>G;265C>G;270T>A] ENSP00000516614.1:p.[Gln86Glu;Arg89Gly;Asn90Lys]
ENST00000706904.1:c.[256C>G;265C>G;270T>A] ENSP00000516615.1:p.[Gln86Glu;Arg89Gly;Asn90Lys]
ENST00000706905.1:c.[256C>G;265C>G;270T>A] ENSP00000516616.1:p.[Gln86Glu;Arg89Gly;Asn90Lys]
ENST00000376809.10:c.[256C>G;265C>G;270T>A] MANE Select ENSP00000366005.5:p.[Gln86Glu;Arg89Gly;Asn90Lys]
ENST00000638375.1:c.[256C>G;265C>G;270T>A] ENSP00000492789.1:p.[Gln86Glu;Arg89Gly;Asn90Lys]
ENST00000376802.2:c.[256C>G;265C>G;270T>A] ENSP00000365998.2:p.[Gln86Glu;Arg89Gly;Asn90Lys]
ENST00000376806.9:c.[256C>G;265C>G;270T>A] ENSP00000366002.5:p.[Gln86Glu;Arg89Gly;Asn90Lys]
ENST00000376809.9:c.[256C>G;265C>G;270T>A] ENSP00000366005.5:p.[Gln86Glu;Arg89Gly;Asn90Lys]
ENST00000396634.5:c.[256C>G;265C>G;270T>A] ENSP00000379873.1:p.[Gln86Glu;Arg89Gly;Asn90Lys]
ENST00000429656.1:n.[115A>T;120G>C;129G>C]
ENST00000461903.1:n.[256C>G;265C>G;270T>A]
ENST00000479320.5:n.[256C>G;265C>G;270T>A]
ENST00000495183.5:n.[258C>G;267C>G;272T>A]
ENST00000496081.5:n.[177+85C>G;177+94C>G;177+99T>A]
NM_002116.7:c.[256C>G;265C>G;270T>A] NP_002107.3:p.[Gln86Glu;Arg89Gly;Asn90Lys]
NM_002116.8:c.[256C>G;265C>G;270T>A] MANE Select NP_002107.3:p.[Gln86Glu;Arg89Gly;Asn90Lys]