Canonical Allele Identifier: CA1618521010

Gene: HLA-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945690G= , CM000668.2:g.29945690G=	GRCh38
NC_000006.11:g.29913467G= , CM000668.1:g.29913467G=	GRCh37
NC_000006.10:g.30021446G=	NCBI36
NG_029217.2:g.8226G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.1216G=	ENSP00000492789.2:n.1216G=
ENST00000706892.1:n.3042G=
ENST00000706893.1:c.*317G=	ENSP00000516609.1:n.*317G=
ENST00000706894.1:c.*317G=	ENSP00000516610.1:n.*317G=
ENST00000706895.1:n.2322G=
ENST00000706896.1:n.2629G=
ENST00000706897.1:n.2051G=
ENST00000706898.1:c.*235G=	ENSP00000516611.1:n.*235G=
ENST00000706899.1:n.2187G=
ENST00000706900.1:c.*235G=	ENSP00000516617.1:n.*235G=
ENST00000706901.1:c.*235G=	ENSP00000516612.1:n.*235G=
ENST00000706902.1:c.1093+409G=	ENSP00000516613.1:n.1093+409G=
ENST00000706903.1:c.*124+111G=	ENSP00000516614.1:n.*124+111G=
ENST00000706904.1:c.1093+409G=	ENSP00000516615.1:n.1093+409G=
ENST00000706905.1:c.*235G=	ENSP00000516616.1:n.*235G=
ENST00000376809.10:c.*235G= MANE Select	ENSP00000366005.5:n.*235G=
ENST00000376802.2:c.*235G=	ENSP00000365998.2:n.*235G=
ENST00000376806.9:c.*235G=	ENSP00000366002.5:n.*235G=
ENST00000376809.9:c.*235G=	ENSP00000366005.5:n.*235G=
ENST00000396634.5:c.*235G=	ENSP00000379873.1:n.*235G=
ENST00000495183.5:n.1572G=
ENST00000496081.5:n.1592G=
NM_002116.7:c.*235G=	NP_002107.3:n.*235G=
NM_002116.8:c.*235G= MANE Select	NP_002107.3:n.*235G=