Canonical Allele Identifier: CA1618520497

Gene: HLA-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945292G= , CM000668.2:g.29945292G=	GRCh38
NC_000006.11:g.29913069G= , CM000668.1:g.29913069G=	GRCh37
NC_000006.10:g.30021048G=	NCBI36
NG_029217.2:g.7828G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.976+11G=	ENSP00000492789.2:n.976+11G=
ENST00000706892.1:n.2644G=
ENST00000706893.1:c.*77+11G=	ENSP00000516609.1:n.*77+11G=
ENST00000706894.1:c.1104G=	ENSP00000516610.1:p.Leu368=
ENST00000706895.1:n.1924G=
ENST00000706896.1:n.2389+11G=
ENST00000706897.1:n.1811+11G=
ENST00000706898.1:c.1111+11G=	ENSP00000516611.1:n.1111+11G=
ENST00000706899.1:n.1947+11G=
ENST00000706900.1:c.1009+11G=	ENSP00000516617.1:n.1009+11G=
ENST00000706901.1:c.1093+11G=	ENSP00000516612.1:n.1093+11G=
ENST00000706902.1:c.1093+11G=	ENSP00000516613.1:n.1093+11G=
ENST00000706903.1:c.1093+11G=	ENSP00000516614.1:n.1093+11G=
ENST00000706904.1:c.1093+11G=	ENSP00000516615.1:n.1093+11G=
ENST00000706905.1:c.1093+11G=	ENSP00000516616.1:n.1093+11G=
ENST00000376809.10:c.1093+11G= MANE Select	ENSP00000366005.5:n.1093+11G=
ENST00000376802.2:c.896-159G=	ENSP00000365998.2:n.896-159G=
ENST00000376806.9:c.1111+11G=	ENSP00000366002.5:n.1111+11G=
ENST00000376809.9:c.1093+11G=	ENSP00000366005.5:n.1093+11G=
ENST00000396634.5:c.1093+11G=	ENSP00000379873.1:n.1093+11G=
ENST00000495183.5:n.1332+11G=
ENST00000496081.5:n.1352+11G=
NM_002116.7:c.1093+11G=	NP_002107.3:n.1093+11G=
NM_002116.8:c.1093+11G= MANE Select	NP_002107.3:n.1093+11G=