Canonical Allele Identifier: CA1618520537

Gene: HLA-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945317T= , CM000668.2:g.29945317T=	GRCh38
NC_000006.11:g.29913094T= , CM000668.1:g.29913094T=	GRCh37
NC_000006.10:g.30021073T=	NCBI36
NG_029217.2:g.7853T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.976+36T=	ENSP00000492789.2:n.976+36T=
ENST00000706892.1:n.2669T=
ENST00000706893.1:c.*77+36T=	ENSP00000516609.1:n.*77+36T=
ENST00000706894.1:c.1129T=	ENSP00000516610.1:p.Trp377=
ENST00000706895.1:n.1949T=
ENST00000706896.1:n.2389+36T=
ENST00000706897.1:n.1811+36T=
ENST00000706898.1:c.1111+36T=	ENSP00000516611.1:n.1111+36T=
ENST00000706899.1:n.1947+36T=
ENST00000706900.1:c.1009+36T=	ENSP00000516617.1:n.1009+36T=
ENST00000706901.1:c.1093+36T=	ENSP00000516612.1:n.1093+36T=
ENST00000706902.1:c.1093+36T=	ENSP00000516613.1:n.1093+36T=
ENST00000706903.1:c.1093+36T=	ENSP00000516614.1:n.1093+36T=
ENST00000706904.1:c.1093+36T=	ENSP00000516615.1:n.1093+36T=
ENST00000706905.1:c.1093+36T=	ENSP00000516616.1:n.1093+36T=
ENST00000376809.10:c.1093+36T= MANE Select	ENSP00000366005.5:n.1093+36T=
ENST00000376802.2:c.896-134T=	ENSP00000365998.2:n.896-134T=
ENST00000376806.9:c.1111+36T=	ENSP00000366002.5:n.1111+36T=
ENST00000376809.9:c.1093+36T=	ENSP00000366005.5:n.1093+36T=
ENST00000396634.5:c.1093+36T=	ENSP00000379873.1:n.1093+36T=
ENST00000495183.5:n.1332+36T=
ENST00000496081.5:n.1352+36T=
NM_002116.7:c.1093+36T=	NP_002107.3:n.1093+36T=
NM_002116.8:c.1093+36T= MANE Select	NP_002107.3:n.1093+36T=