Canonical Allele Identifier: CA917711616

Gene: HLA-C

Linked Data

• dbSNP Id: rs1562022633

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31270153_31270154insAGA , CM000668.2:g.31270153_31270154insAGA	GRCh38
NC_000006.11:g.31237930_31237931insAGA , CM000668.1:g.31237930_31237931insAGA	GRCh37
NC_000006.10:g.31345909_31345910insAGA	NCBI36
NG_029422.2:g.6978_6979insTCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.895+56_895+57insTCT MANE Select	ENSP00000365402.5:n.895+56_895+57insTCT
ENST00000376228.9:c.895+56_895+57insTCT	ENSP00000365402.5:n.895+56_895+57insTCT
ENST00000376237.8:c.*482+56_*482+57insTCT	ENSP00000365412.4:n.*482+56_*482+57insTCT
ENST00000383329.7:c.895+56_895+57insTCT	ENSP00000372819.3:n.895+56_895+57insTCT
ENST00000470363.5:n.213+56_213+57insTCT
ENST00000487245.5:n.1254+56_1254+57insTCT
NM_002117.5:c.895+56_895+57insTCT	NP_002108.4:n.895+56_895+57insTCT
NM_002117.6:c.895+56_895+57insTCT MANE Select	NP_002108.4:n.895+56_895+57insTCT