Canonical Allele Identifier: CA1618519521

Gene: HLA-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29944537C= , CM000668.2:g.29944537C=	GRCh38
NC_000006.11:g.29912314C= , CM000668.1:g.29912314C=	GRCh37
NC_000006.10:g.30020293C=	NCBI36
NG_029217.2:g.7073C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.895+140C=	ENSP00000492789.2:n.895+140C=
ENST00000706892.1:n.1889C=
ENST00000706893.1:c.967C=	ENSP00000516609.1:p.His323=
ENST00000706894.1:c.933C=	ENSP00000516610.1:p.Ile311=
ENST00000706895.1:n.1311C=
ENST00000706896.1:n.1787C=
ENST00000706897.1:n.1209C=
ENST00000706898.1:c.933C=	ENSP00000516611.1:p.Ile311=
ENST00000706899.1:n.1787C=
ENST00000706900.1:c.849C=	ENSP00000516617.1:p.Ile283=
ENST00000706901.1:c.933C=	ENSP00000516612.1:p.Ile311=
ENST00000706902.1:c.933C=	ENSP00000516613.1:p.Ile311=
ENST00000706903.1:c.933C=	ENSP00000516614.1:p.Ile311=
ENST00000706904.1:c.933C=	ENSP00000516615.1:p.Ile311=
ENST00000706905.1:c.933C=	ENSP00000516616.1:p.Ile311=
ENST00000376809.10:c.933C= MANE Select	ENSP00000366005.5:p.Ile311=
ENST00000638375.1:c.895+140C=	ENSP00000492789.1:n.895+140C=
ENST00000376802.2:c.895+140C=	ENSP00000365998.2:n.895+140C=
ENST00000376806.9:c.933C=	ENSP00000366002.5:p.Ile311=
ENST00000376809.9:c.933C=	ENSP00000366005.5:p.Ile311=
ENST00000396634.5:c.933C=	ENSP00000379873.1:p.Ile311=
ENST00000461903.1:n.1174C=
ENST00000479320.5:n.1174C=
ENST00000495183.5:n.1176C=
ENST00000496081.5:n.750C=
NM_002116.7:c.933C=	NP_002107.3:p.Ile311=
NM_002116.8:c.933C= MANE Select	NP_002107.3:p.Ile311=