Canonical Allele Identifier: CA2677950621

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31270186-GTGA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31270187_31270189del , CM000668.2:g.31270187_31270189del	GRCh38
NC_000006.11:g.31237964_31237966del , CM000668.1:g.31237964_31237966del	GRCh37
NC_000006.10:g.31345943_31345945del	NCBI36
NG_029422.2:g.6943_6945del

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.895+21_895+23del MANE Select	ENSP00000365402.5:n.895+21_895+23del
ENST00000376228.9:c.895+21_895+23del	ENSP00000365402.5:n.895+21_895+23del
ENST00000376237.8:c.*482+21_*482+23del	ENSP00000365412.4:n.*482+21_*482+23del
ENST00000383329.7:c.895+21_895+23del	ENSP00000372819.3:n.895+21_895+23del
ENST00000470363.5:n.213+21_213+23del
ENST00000487245.5:n.1254+21_1254+23del
NM_002117.5:c.895+21_895+23del	NP_002108.4:n.895+21_895+23del
NM_002117.6:c.895+21_895+23del MANE Select	NP_002108.4:n.895+21_895+23del