Canonical Allele Identifier: CA2573333721

Gene: HLA-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.[29942940A>G;29942942G>A;29942944G>C] , CM000668.2:g.[29942940A>G;29942942G>A;29942944G>C]	GRCh38
NC_000006.11:g.[29910717A>G;29910719G>A;29910721G>C] , CM000668.1:g.[29910717A>G;29910719G>A;29910721G>C]	GRCh37
NC_000006.10:g.[30018696A>G;30018698G>A;30018700G>C]	NCBI36
NG_029217.2:g.[5475A>G;5477G>A;5479G>C]

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.[257A>G;259G>A;261G>C]	ENSP00000492789.2:p.[Gln86_Glu87delinsArgLys;Glu87Asp]
ENST00000706892.1:n.[533A>G;535G>A;537G>C]
ENST00000706893.1:c.[257A>G;259G>A;261G>C]	ENSP00000516609.1:p.[Gln86_Glu87delinsArgLys;Glu87Asp]
ENST00000706894.1:c.[257A>G;259G>A;261G>C]	ENSP00000516610.1:p.[Gln86_Glu87delinsArgLys;Glu87Asp]
ENST00000706895.1:n.[533A>G;535G>A;537G>C]
ENST00000706896.1:n.[533A>G;535G>A;537G>C]
ENST00000706897.1:n.[533A>G;535G>A;537G>C]
ENST00000706898.1:c.[257A>G;259G>A;261G>C]	ENSP00000516611.1:p.[Gln86_Glu87delinsArgLys;Glu87Asp]
ENST00000706899.1:n.[533A>G;535G>A;537G>C]
ENST00000706900.1:c.[173A>G;175G>A;177G>C]	ENSP00000516617.1:p.[Gln58Arg;Glu59Asn]
ENST00000706901.1:c.[257A>G;259G>A;261G>C]	ENSP00000516612.1:p.[Gln86_Glu87delinsArgLys;Glu87Asp]
ENST00000706902.1:c.[257A>G;259G>A;261G>C]	ENSP00000516613.1:p.[Gln86_Glu87delinsArgLys;Glu87Asp]
ENST00000706903.1:c.[257A>G;259G>A;261G>C]	ENSP00000516614.1:p.[Gln86_Glu87delinsArgLys;Glu87Asp]
ENST00000706904.1:c.[257A>G;259G>A;261G>C]	ENSP00000516615.1:p.[Gln86_Glu87delinsArgLys;Glu87Asp]
ENST00000706905.1:c.[257A>G;259G>A;261G>C]	ENSP00000516616.1:p.[Gln86Arg;Glu87Lys;Glu87Asp]
ENST00000376809.10:c.[257A>G;259G>A;261G>C] MANE Select	ENSP00000366005.5:p.[Gln86Arg;Glu87Thr]
ENST00000638375.1:c.[257A>G;259G>A;261G>C]	ENSP00000492789.1:p.[Gln86_Glu87delinsArgLys;Glu87Asp]
ENST00000376802.2:c.[257A>G;259G>A;261G>C]	ENSP00000365998.2:p.[Gln86Arg;Glu87Lys;Glu87Asp]
ENST00000376806.9:c.[257A>G;259G>A;261G>C]	ENSP00000366002.5:p.[Gln86_Glu87delinsArgLys;Glu87Asp]
ENST00000376809.9:c.[257A>G;259G>A;261G>C]	ENSP00000366005.5:p.[Gln86_Glu87delinsArgLys;Glu87Asp]
ENST00000396634.5:c.[257A>G;259G>A;261G>C]	ENSP00000379873.1:p.[Gln86Arg;Glu87Lys;Glu87Asp]
ENST00000429656.1:n.[124C>G;126C>T;128T>C]
ENST00000461903.1:n.[257A>G;259G>A;261G>C]
ENST00000479320.5:n.[257A>G;259G>A;261G>C]
ENST00000495183.5:n.[259A>G;261G>A;263G>C]
ENST00000496081.5:n.[177+86A>G;177+88G>A;177+90G>C]
NM_002116.7:c.[257A>G;259G>A;261G>C]	NP_002107.3:p.[Gln86_Glu87delinsArgLys;Glu87Asp]
NM_002116.8:c.[257A>G;259G>A;261G>C] MANE Select	NP_002107.3:p.[Gln86Arg;Glu87Thr]