Canonical Allele Identifier: CA1619080406

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271196T= , CM000668.2:g.31271196T=	GRCh38
NC_000006.11:g.31238973T= , CM000668.1:g.31238973T=	GRCh37
NC_000006.10:g.31346952T=	NCBI36
NG_029422.2:g.5936A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.496A= MANE Select	ENSP00000365402.5:p.Ile166=
ENST00000376228.9:c.496A=	ENSP00000365402.5:p.Ile166=
ENST00000376237.8:c.*83A=	ENSP00000365412.4:n.*83A=
ENST00000383329.7:c.496A=	ENSP00000372819.3:p.Ile166=
ENST00000415537.1:c.494A=
ENST00000484378.1:n.765A=
ENST00000487245.5:n.855A=
ENST00000495835.1:n.685A=
NM_002117.5:c.496A=	NP_002108.4:p.Ile166=
NM_002117.6:c.496A= MANE Select	NP_002108.4:p.Ile166=