Canonical Allele Identifier: CA1087427784

Gene: HLA-C

Linked Data

• dbSNP Id: rs1761351210
• gnomAD v3: 6-31271502-T-TC
• gnomAD v4: 6-31271502-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271502_31271503insC , CM000668.2:g.31271502_31271503insC	GRCh38
NC_000006.11:g.31239279_31239280insC , CM000668.1:g.31239279_31239280insC	GRCh37
NC_000006.10:g.31347258_31347259insC	NCBI36
NG_029422.2:g.5629_5630insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.343+96_343+97insG MANE Select	ENSP00000365402.5:n.343+96_343+97insG
ENST00000376228.9:c.343+96_343+97insG	ENSP00000365402.5:n.343+96_343+97insG
ENST00000376237.8:c.343+96_343+97insG	ENSP00000365412.4:n.343+96_343+97insG
ENST00000383329.7:c.343+96_343+97insG	ENSP00000372819.3:n.343+96_343+97insG
ENST00000415537.1:c.341+96_341+97insG
ENST00000484378.1:n.458_459insG
ENST00000487245.5:n.548_549insG
ENST00000495835.1:n.532+96_532+97insG
NM_002117.5:c.343+96_343+97insG	NP_002108.4:n.343+96_343+97insG
NM_002117.6:c.343+96_343+97insG MANE Select	NP_002108.4:n.343+96_343+97insG