Canonical Allele Identifier: CA2677949558

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31269261-CCAAT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269265_31269268del , CM000668.2:g.31269265_31269268del	GRCh38
NC_000006.11:g.31237042_31237045del , CM000668.1:g.31237042_31237045del	GRCh37
NC_000006.10:g.31345021_31345024del	NCBI36
NG_029422.2:g.7867_7870del

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.1096+73_1096+76del MANE Select	ENSP00000365402.5:n.1096+73_1096+76del
ENST00000376228.9:c.1096+73_1096+76del	ENSP00000365402.5:n.1096+73_1096+76del
ENST00000376237.8:c.*683+73_*683+76del	ENSP00000365412.4:n.*683+73_*683+76del
ENST00000383329.7:c.1114+73_1114+76del	ENSP00000372819.3:n.1114+73_1114+76del
ENST00000466892.5:n.329+73_329+76del
ENST00000470363.5:n.854+73_854+76del
ENST00000487245.5:n.1455+73_1455+76del
NM_002117.5:c.1096+73_1096+76del	NP_002108.4:n.1096+73_1096+76del
NM_002117.6:c.1096+73_1096+76del MANE Select	NP_002108.4:n.1096+73_1096+76del