Canonical Allele Identifier: CA1619080644

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271485G= , CM000668.2:g.31271485G=	GRCh38
NC_000006.11:g.31239262G= , CM000668.1:g.31239262G=	GRCh37
NC_000006.10:g.31347241G=	NCBI36
NG_029422.2:g.5647C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.343+114C= MANE Select	ENSP00000365402.5:n.343+114C=
ENST00000376228.9:c.343+114C=	ENSP00000365402.5:n.343+114C=
ENST00000376237.8:c.343+114C=	ENSP00000365412.4:n.343+114C=
ENST00000383329.7:c.343+114C=	ENSP00000372819.3:n.343+114C=
ENST00000415537.1:c.341+114C=
ENST00000484378.1:n.476C=
ENST00000487245.5:n.566C=
ENST00000495835.1:n.532+114C=
NM_002117.5:c.343+114C=	NP_002108.4:n.343+114C=
NM_002117.6:c.343+114C= MANE Select	NP_002108.4:n.343+114C=