Canonical Allele Identifier: CA1619079126

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31270153_31270156delinsCCAG , CM000668.2:g.31270153_31270156delinsCCAG	GRCh38
NC_000006.11:g.31237930_31237933delinsCCAG , CM000668.1:g.31237930_31237933delinsCCAG	GRCh37
NC_000006.10:g.31345909_31345912delinsCCAG	NCBI36
NG_029422.2:g.6976_6979delinsCTGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.895+54_895+57delinsCTGG MANE Select	ENSP00000365402.5:n.895+54_895+57delinsCTGG
ENST00000376228.9:c.895+54_895+57delinsCTGG	ENSP00000365402.5:n.895+54_895+57delinsCTGG
ENST00000376237.8:c.*482+54_*482+57delinsCTGG	ENSP00000365412.4:n.*482+54_*482+57delinsCTGG
ENST00000383329.7:c.895+54_895+57delinsCTGG	ENSP00000372819.3:n.895+54_895+57delinsCTGG
ENST00000470363.5:n.213+54_213+57delinsCTGG
ENST00000487245.5:n.1254+54_1254+57delinsCTGG
NM_002117.5:c.895+54_895+57delinsCTGG	NP_002108.4:n.895+54_895+57delinsCTGG
NM_002117.6:c.895+54_895+57delinsCTGG MANE Select	NP_002108.4:n.895+54_895+57delinsCTGG