Canonical Allele Identifier: CA2677949651

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31269345-AGT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269347_31269348del , CM000668.2:g.31269347_31269348del	GRCh38
NC_000006.11:g.31237124_31237125del , CM000668.1:g.31237124_31237125del	GRCh37
NC_000006.10:g.31345103_31345104del	NCBI36
NG_029422.2:g.7785_7786del

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.1087_1088del MANE Select	ENSP00000365402.5:p.Thr363LeufsTer2
ENST00000376228.9:c.1087_1088del	ENSP00000365402.5:p.Thr363LeufsTer2
ENST00000376237.8:c.*674_*675del	ENSP00000365412.4:n.*674_*675del
ENST00000383329.7:c.1105_1106del	ENSP00000372819.3:p.Thr369LeufsTer2
ENST00000466892.5:n.320_321del
ENST00000470363.5:n.845_846del
ENST00000487245.5:n.1446_1447del
NM_002117.5:c.1087_1088del	NP_002108.4:p.Thr363LeufsTer2
NM_002117.6:c.1087_1088del MANE Select	NP_002108.4:p.Thr363LeufsTer2