Canonical Allele Identifier: CA2677949563

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31269269-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269270dup , CM000668.2:g.31269270dup	GRCh38
NC_000006.11:g.31237047dup , CM000668.1:g.31237047dup	GRCh37
NC_000006.10:g.31345026dup	NCBI36
NG_029422.2:g.7862dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.1096+68dup MANE Select	ENSP00000365402.5:n.1096+68dup
ENST00000376228.9:c.1096+68dup	ENSP00000365402.5:n.1096+68dup
ENST00000376237.8:c.*683+68dup	ENSP00000365412.4:n.*683+68dup
ENST00000383329.7:c.1114+68dup	ENSP00000372819.3:n.1114+68dup
ENST00000466892.5:n.329+68dup
ENST00000470363.5:n.854+68dup
ENST00000487245.5:n.1455+68dup
NM_002117.5:c.1096+68dup	NP_002108.4:n.1096+68dup
NM_002117.6:c.1096+68dup MANE Select	NP_002108.4:n.1096+68dup