Canonical Allele Identifier: CA2677949791

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31269514-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269515del , CM000668.2:g.31269515del	GRCh38
NC_000006.11:g.31237292del , CM000668.1:g.31237292del	GRCh37
NC_000006.10:g.31345271del	NCBI36
NG_029422.2:g.7617del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.1026del MANE Select	ENSP00000365402.5:p.Ser344AlafsTer?
ENST00000376228.9:c.1026del	ENSP00000365402.5:p.Ser344AlafsTer?
ENST00000376237.8:c.*613del	ENSP00000365412.4:n.*613del
ENST00000383329.7:c.1044del	ENSP00000372819.3:p.Ser350AlafsTer?
ENST00000466892.5:n.152del
ENST00000470363.5:n.784del
ENST00000487245.5:n.1385del
NM_002117.5:c.1026del	NP_002108.4:p.Ser344AlafsTer?
NM_002117.6:c.1026del MANE Select	NP_002108.4:p.Ser344AlafsTer?