Canonical Allele Identifier: CA2677949758

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31269460-G-GGGTA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269460_31269461insGGTA , CM000668.2:g.31269460_31269461insGGTA	GRCh38
NC_000006.11:g.31237237_31237238insGGTA , CM000668.1:g.31237237_31237238insGGTA	GRCh37
NC_000006.10:g.31345216_31345217insGGTA	NCBI36
NG_029422.2:g.7671_7672insTACC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.1048+32_1048+33insTACC MANE Select	ENSP00000365402.5:n.1048+32_1048+33insTACC
ENST00000376228.9:c.1048+32_1048+33insTACC	ENSP00000365402.5:n.1048+32_1048+33insTACC
ENST00000376237.8:c.*635+32_*635+33insTACC	ENSP00000365412.4:n.*635+32_*635+33insTACC
ENST00000383329.7:c.1066+32_1066+33insTACC	ENSP00000372819.3:n.1066+32_1066+33insTACC
ENST00000466892.5:n.206_207insTACC
ENST00000470363.5:n.806+32_806+33insTACC
ENST00000487245.5:n.1407+32_1407+33insTACC
NM_002117.5:c.1048+32_1048+33insTACC	NP_002108.4:n.1048+32_1048+33insTACC
NM_002117.6:c.1048+32_1048+33insTACC MANE Select	NP_002108.4:n.1048+32_1048+33insTACC