Canonical Allele Identifier: CA1087451744

Gene: HLA-C

Linked Data

• dbSNP Id: rs1761144024
• gnomAD v3: 6-31269749-C-CG
• gnomAD v4: 6-31269749-C-CG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269749_31269750insG , CM000668.2:g.31269749_31269750insG	GRCh38
NC_000006.11:g.31237526_31237527insG , CM000668.1:g.31237526_31237527insG	GRCh37
NC_000006.10:g.31345505_31345506insG	NCBI36
NG_029422.2:g.7382_7383insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.1015+216_1015+217insC MANE Select	ENSP00000365402.5:n.1015+216_1015+217insC
ENST00000376228.9:c.1015+216_1015+217insC	ENSP00000365402.5:n.1015+216_1015+217insC
ENST00000376237.8:c.*602+216_*602+217insC	ENSP00000365412.4:n.*602+216_*602+217insC
ENST00000383329.7:c.1016-207_1016-206insC	ENSP00000372819.3:n.1016-207_1016-206insC
ENST00000470363.5:n.549_550insC
ENST00000487245.5:n.1374+216_1374+217insC
NM_002117.5:c.1015+216_1015+217insC	NP_002108.4:n.1015+216_1015+217insC
NM_002117.6:c.1015+216_1015+217insC MANE Select	NP_002108.4:n.1015+216_1015+217insC