Canonical Allele Identifier: CA2677950195

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31269883-AAG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269884_31269885del , CM000668.2:g.31269884_31269885del	GRCh38
NC_000006.11:g.31237661_31237662del , CM000668.1:g.31237661_31237662del	GRCh37
NC_000006.10:g.31345640_31345641del	NCBI36
NG_029422.2:g.7247_7248del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.1015+81_1015+82del MANE Select	ENSP00000365402.5:n.1015+81_1015+82del
ENST00000376228.9:c.1015+81_1015+82del	ENSP00000365402.5:n.1015+81_1015+82del
ENST00000376237.8:c.*602+81_*602+82del	ENSP00000365412.4:n.*602+81_*602+82del
ENST00000383329.7:c.1015+81_1015+82del	ENSP00000372819.3:n.1015+81_1015+82del
ENST00000470363.5:n.414_415del
ENST00000487245.5:n.1374+81_1374+82del
NM_002117.5:c.1015+81_1015+82del	NP_002108.4:n.1015+81_1015+82del
NM_002117.6:c.1015+81_1015+82del MANE Select	NP_002108.4:n.1015+81_1015+82del