Canonical Allele Identifier: CA1618520627

Gene: HLA-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945398T= , CM000668.2:g.29945398T=	GRCh38
NC_000006.11:g.29913175T= , CM000668.1:g.29913175T=	GRCh37
NC_000006.10:g.30021154T=	NCBI36
NG_029217.2:g.7934T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.977-53T=	ENSP00000492789.2:n.977-53T=
ENST00000706892.1:n.2750T=
ENST00000706893.1:c.*78-53T=	ENSP00000516609.1:n.*78-53T=
ENST00000706894.1:c.*25T=	ENSP00000516610.1:n.*25T=
ENST00000706895.1:n.2030T=
ENST00000706896.1:n.2390-53T=
ENST00000706897.1:n.1812-53T=
ENST00000706898.1:c.1112-53T=	ENSP00000516611.1:n.1112-53T=
ENST00000706899.1:n.1948-53T=
ENST00000706900.1:c.1010-53T=	ENSP00000516617.1:n.1010-53T=
ENST00000706901.1:c.1094-53T=	ENSP00000516612.1:n.1094-53T=
ENST00000706902.1:c.1093+117T=	ENSP00000516613.1:n.1093+117T=
ENST00000706903.1:c.1094-53T=	ENSP00000516614.1:n.1094-53T=
ENST00000706904.1:c.1093+117T=	ENSP00000516615.1:n.1093+117T=
ENST00000706905.1:c.1094-53T=	ENSP00000516616.1:n.1094-53T=
ENST00000376809.10:c.1094-53T= MANE Select	ENSP00000366005.5:n.1094-53T=
ENST00000376802.2:c.896-53T=	ENSP00000365998.2:n.896-53T=
ENST00000376806.9:c.1112-53T=	ENSP00000366002.5:n.1112-53T=
ENST00000376809.9:c.1094-53T=	ENSP00000366005.5:n.1094-53T=
ENST00000396634.5:c.1094-53T=	ENSP00000379873.1:n.1094-53T=
ENST00000495183.5:n.1333-53T=
ENST00000496081.5:n.1353-53T=
NM_002116.7:c.1094-53T=	NP_002107.3:n.1094-53T=
NM_002116.8:c.1094-53T= MANE Select	NP_002107.3:n.1094-53T=