Canonical Allele Identifier: CA2677949777

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31269479-CCG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269481_31269482del , CM000668.2:g.31269481_31269482del	GRCh38
NC_000006.11:g.31237258_31237259del , CM000668.1:g.31237258_31237259del	GRCh37
NC_000006.10:g.31345237_31345238del	NCBI36
NG_029422.2:g.7651_7652del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.1048+12_1048+13del MANE Select	ENSP00000365402.5:n.1048+12_1048+13del
ENST00000376228.9:c.1048+12_1048+13del	ENSP00000365402.5:n.1048+12_1048+13del
ENST00000376237.8:c.*635+12_*635+13del	ENSP00000365412.4:n.*635+12_*635+13del
ENST00000383329.7:c.1066+12_1066+13del	ENSP00000372819.3:n.1066+12_1066+13del
ENST00000466892.5:n.186_187del
ENST00000470363.5:n.806+12_806+13del
ENST00000487245.5:n.1407+12_1407+13del
NM_002117.5:c.1048+12_1048+13del	NP_002108.4:n.1048+12_1048+13del
NM_002117.6:c.1048+12_1048+13del MANE Select	NP_002108.4:n.1048+12_1048+13del