Canonical Allele Identifier: CA1619078882

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31270043G= , CM000668.2:g.31270043G=	GRCh38
NC_000006.11:g.31237820G= , CM000668.1:g.31237820G=	GRCh37
NC_000006.10:g.31345799G=	NCBI36
NG_029422.2:g.7089C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.938C= MANE Select	ENSP00000365402.5:p.Ala313=
ENST00000376228.9:c.938C=	ENSP00000365402.5:p.Ala313=
ENST00000376237.8:c.*525C=	ENSP00000365412.4:n.*525C=
ENST00000383329.7:c.938C=	ENSP00000372819.3:p.Ala313=
ENST00000470363.5:n.256C=
ENST00000487245.5:n.1297C=
NM_002117.5:c.938C=	NP_002108.4:p.Ala313=
NM_002117.6:c.938C= MANE Select	NP_002108.4:p.Ala313=