Canonical Allele Identifier: CA2677949765

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31269465-C-CACCTA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269465_31269466insACCTA , CM000668.2:g.31269465_31269466insACCTA	GRCh38
NC_000006.11:g.31237242_31237243insACCTA , CM000668.1:g.31237242_31237243insACCTA	GRCh37
NC_000006.10:g.31345221_31345222insACCTA	NCBI36
NG_029422.2:g.7666_7667insTAGGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.1048+27_1048+28insTAGGT MANE Select	ENSP00000365402.5:n.1048+27_1048+28insTAGGT
ENST00000376228.9:c.1048+27_1048+28insTAGGT	ENSP00000365402.5:n.1048+27_1048+28insTAGGT
ENST00000376237.8:c.*635+27_*635+28insTAGGT	ENSP00000365412.4:n.*635+27_*635+28insTAGGT
ENST00000383329.7:c.1066+27_1066+28insTAGGT	ENSP00000372819.3:n.1066+27_1066+28insTAGGT
ENST00000466892.5:n.201_202insTAGGT
ENST00000470363.5:n.806+27_806+28insTAGGT
ENST00000487245.5:n.1407+27_1407+28insTAGGT
NM_002117.5:c.1048+27_1048+28insTAGGT	NP_002108.4:n.1048+27_1048+28insTAGGT
NM_002117.6:c.1048+27_1048+28insTAGGT MANE Select	NP_002108.4:n.1048+27_1048+28insTAGGT