Canonical Allele Identifier: CA1619079156

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31270162C= , CM000668.2:g.31270162C=	GRCh38
NC_000006.11:g.31237939C= , CM000668.1:g.31237939C=	GRCh37
NC_000006.10:g.31345918C=	NCBI36
NG_029422.2:g.6970G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.895+48G= MANE Select	ENSP00000365402.5:n.895+48G=
ENST00000376228.9:c.895+48G=	ENSP00000365402.5:n.895+48G=
ENST00000376237.8:c.*482+48G=	ENSP00000365412.4:n.*482+48G=
ENST00000383329.7:c.895+48G=	ENSP00000372819.3:n.895+48G=
ENST00000470363.5:n.213+48G=
ENST00000487245.5:n.1254+48G=
NM_002117.5:c.895+48G=	NP_002108.4:n.895+48G=
NM_002117.6:c.895+48G= MANE Select	NP_002108.4:n.895+48G=