Canonical Allele Identifier: CA2711332410

Gene: HLA-C

Linked Data

• dbSNP Id: rs2113902168

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269420_31269421insAGCTC , CM000668.2:g.31269420_31269421insAGCTC	GRCh38
NC_000006.11:g.31237197_31237198insAGCTC , CM000668.1:g.31237197_31237198insAGCTC	GRCh37
NC_000006.10:g.31345176_31345177insAGCTC	NCBI36
NG_029422.2:g.7712_7713insAGCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.1049-35_1049-34insAGCTG MANE Select	ENSP00000365402.5:n.1049-35_1049-34insAGCTG
ENST00000376228.9:c.1049-35_1049-34insAGCTG	ENSP00000365402.5:n.1049-35_1049-34insAGCTG
ENST00000376237.8:c.*636-35_*636-34insAGCTG	ENSP00000365412.4:n.*636-35_*636-34insAGCTG
ENST00000383329.7:c.1067-35_1067-34insAGCTG	ENSP00000372819.3:n.1067-35_1067-34insAGCTG
ENST00000466892.5:n.247_248insAGCTG
ENST00000470363.5:n.807-35_807-34insAGCTG
ENST00000487245.5:n.1408-35_1408-34insAGCTG
NM_002117.5:c.1049-35_1049-34insAGCTG	NP_002108.4:n.1049-35_1049-34insAGCTG
NM_002117.6:c.1049-35_1049-34insAGCTG MANE Select	NP_002108.4:n.1049-35_1049-34insAGCTG