Canonical Allele Identifier: CA1619078688

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269992G= , CM000668.2:g.31269992G=	GRCh38
NC_000006.11:g.31237769G= , CM000668.1:g.31237769G=	GRCh37
NC_000006.10:g.31345748G=	NCBI36
NG_029422.2:g.7140C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.989C= MANE Select	ENSP00000365402.5:p.Ala330=
ENST00000376228.9:c.989C=	ENSP00000365402.5:p.Ala330=
ENST00000376237.8:c.*576C=	ENSP00000365412.4:n.*576C=
ENST00000383329.7:c.989C=	ENSP00000372819.3:p.Ala330=
ENST00000470363.5:n.307C=
ENST00000487245.5:n.1348C=
NM_002117.5:c.989C=	NP_002108.4:p.Ala330=
NM_002117.6:c.989C= MANE Select	NP_002108.4:p.Ala330=