Canonical Allele Identifier: CA1619078398

Gene: HLA-C

Linked Data

• dbSNP Id: rs1761147479

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269785_31269786insG , CM000668.2:g.31269785_31269786insG	GRCh38
NC_000006.11:g.31237562_31237563insG , CM000668.1:g.31237562_31237563insG	GRCh37
NC_000006.10:g.31345541_31345542insG	NCBI36
NG_029422.2:g.7346_7347insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.1015+180_1015+181insC MANE Select	ENSP00000365402.5:n.1015+180_1015+181insC
ENST00000376228.9:c.1015+180_1015+181insC	ENSP00000365402.5:n.1015+180_1015+181insC
ENST00000376237.8:c.*602+180_*602+181insC	ENSP00000365412.4:n.*602+180_*602+181insC
ENST00000383329.7:c.1015+180_1015+181insC	ENSP00000372819.3:n.1015+180_1015+181insC
ENST00000470363.5:n.513_514insC
ENST00000487245.5:n.1374+180_1374+181insC
NM_002117.5:c.1015+180_1015+181insC	NP_002108.4:n.1015+180_1015+181insC
NM_002117.6:c.1015+180_1015+181insC MANE Select	NP_002108.4:n.1015+180_1015+181insC