Canonical Allele Identifier: CA2677950277

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31269978-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269980del , CM000668.2:g.31269980del	GRCh38
NC_000006.11:g.31237757del , CM000668.1:g.31237757del	GRCh37
NC_000006.10:g.31345736del	NCBI36
NG_029422.2:g.7153del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.1002del MANE Select	ENSP00000365402.5:p.Arg335GlyfsTer?
ENST00000376228.9:c.1002del	ENSP00000365402.5:p.Arg335GlyfsTer?
ENST00000376237.8:c.*589del	ENSP00000365412.4:n.*589del
ENST00000383329.7:c.1002del	ENSP00000372819.3:p.Arg335GlyfsTer?
ENST00000470363.5:n.320del
ENST00000487245.5:n.1361del
NM_002117.5:c.1002del	NP_002108.4:p.Arg335GlyfsTer?
NM_002117.6:c.1002del MANE Select	NP_002108.4:p.Arg335GlyfsTer?