Canonical Allele Identifier: CA1619080432

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271225G= , CM000668.2:g.31271225G=	GRCh38
NC_000006.11:g.31239002G= , CM000668.1:g.31239002G=	GRCh37
NC_000006.10:g.31346981G=	NCBI36
NG_029422.2:g.5907C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.467C= MANE Select	ENSP00000365402.5:p.Ser156=
ENST00000376228.9:c.467C=	ENSP00000365402.5:p.Ser156=
ENST00000376237.8:c.*54C=	ENSP00000365412.4:n.*54C=
ENST00000383329.7:c.467C=	ENSP00000372819.3:p.Ser156=
ENST00000415537.1:c.465C=
ENST00000484378.1:n.736C=
ENST00000487245.5:n.826C=
ENST00000495835.1:n.656C=
NM_002117.5:c.467C=	NP_002108.4:p.Ser156=
NM_002117.6:c.467C= MANE Select	NP_002108.4:p.Ser156=