Canonical Allele Identifier: CA1618520946

Gene: HLA-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945615C= , CM000668.2:g.29945615C=	GRCh38
NC_000006.11:g.29913392C= , CM000668.1:g.29913392C=	GRCh37
NC_000006.10:g.30021371C=	NCBI36
NG_029217.2:g.8151C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.1141C=	ENSP00000492789.2:n.1141C=
ENST00000706892.1:n.2967C=
ENST00000706893.1:c.*242C=	ENSP00000516609.1:n.*242C=
ENST00000706894.1:c.*242C=	ENSP00000516610.1:n.*242C=
ENST00000706895.1:n.2247C=
ENST00000706896.1:n.2554C=
ENST00000706897.1:n.1976C=
ENST00000706898.1:c.*160C=	ENSP00000516611.1:n.*160C=
ENST00000706899.1:n.2112C=
ENST00000706900.1:c.*160C=	ENSP00000516617.1:n.*160C=
ENST00000706901.1:c.*160C=	ENSP00000516612.1:n.*160C=
ENST00000706902.1:c.1093+334C=	ENSP00000516613.1:n.1093+334C=
ENST00000706903.1:c.*124+36C=	ENSP00000516614.1:n.*124+36C=
ENST00000706904.1:c.1093+334C=	ENSP00000516615.1:n.1093+334C=
ENST00000706905.1:c.*160C=	ENSP00000516616.1:n.*160C=
ENST00000376809.10:c.*160C= MANE Select	ENSP00000366005.5:n.*160C=
ENST00000376802.2:c.*160C=	ENSP00000365998.2:n.*160C=
ENST00000376806.9:c.*160C=	ENSP00000366002.5:n.*160C=
ENST00000376809.9:c.*160C=	ENSP00000366005.5:n.*160C=
ENST00000396634.5:c.*160C=	ENSP00000379873.1:n.*160C=
ENST00000495183.5:n.1497C=
ENST00000496081.5:n.1517C=
NM_002116.7:c.*160C=	NP_002107.3:n.*160C=
NM_002116.8:c.*160C= MANE Select	NP_002107.3:n.*160C=