Canonical Allele Identifier: CA1618522793

Gene: HLA-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29942533G= , CM000668.2:g.29942533G=	GRCh38
NC_000006.11:g.29910310G= , CM000668.1:g.29910310G=	GRCh37
NC_000006.10:g.30018289G=	NCBI36
NG_029217.2:g.5068G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706892.1:n.256G=
ENST00000706893.1:c.-21G=	ENSP00000516609.1:n.-21G=
ENST00000706894.1:c.-21G=	ENSP00000516610.1:n.-21G=
ENST00000706895.1:n.256G=
ENST00000706896.1:n.256G=
ENST00000706897.1:n.256G=
ENST00000706898.1:c.-21G=	ENSP00000516611.1:n.-21G=
ENST00000706899.1:n.256G=
ENST00000706901.1:c.-21G=	ENSP00000516612.1:n.-21G=
ENST00000706902.1:c.-21G=	ENSP00000516613.1:n.-21G=
ENST00000706903.1:c.-21G=	ENSP00000516614.1:n.-21G=
ENST00000706904.1:c.-21G=	ENSP00000516615.1:n.-21G=
ENST00000706905.1:c.-21G=	ENSP00000516616.1:n.-21G=
ENST00000376809.10:c.-21G= MANE Select	ENSP00000366005.5:n.-21G=
ENST00000376806.9:c.-21G=	ENSP00000366002.5:n.-21G=
ENST00000376809.9:c.-21G=	ENSP00000366005.5:n.-21G=
ENST00000396634.5:c.-21G=	ENSP00000379873.1:n.-21G=
ENST00000429656.1:n.535C=
NM_002116.7:c.-21G=	NP_002107.3:n.-21G=
NM_002116.8:c.-21G= MANE Select	NP_002107.3:n.-21G=