Canonical Allele Identifier: CA1619078630

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269983C= , CM000668.2:g.31269983C=	GRCh38
NC_000006.11:g.31237760C= , CM000668.1:g.31237760C=	GRCh37
NC_000006.10:g.31345739C=	NCBI36
NG_029422.2:g.7149G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.998G= MANE Select	ENSP00000365402.5:p.Cys333=
ENST00000376228.9:c.998G=	ENSP00000365402.5:p.Cys333=
ENST00000376237.8:c.*585G=	ENSP00000365412.4:n.*585G=
ENST00000383329.7:c.998G=	ENSP00000372819.3:p.Cys333=
ENST00000470363.5:n.316G=
ENST00000487245.5:n.1357G=
NM_002117.5:c.998G=	NP_002108.4:p.Cys333=
NM_002117.6:c.998G= MANE Select	NP_002108.4:p.Cys333=