Canonical Allele Identifier: CA2711332460

Gene: HLA-C

Linked Data

• dbSNP Id: rs2113902240

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269439_31269446del , CM000668.2:g.31269439_31269446del	GRCh38
NC_000006.11:g.31237216_31237223del , CM000668.1:g.31237216_31237223del	GRCh37
NC_000006.10:g.31345195_31345202del	NCBI36
NG_029422.2:g.7686_7693del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.1048+47_1049-54del MANE Select	ENSP00000365402.5:n.1048+47_1049-54del
ENST00000376228.9:c.1048+47_1049-54del	ENSP00000365402.5:n.1048+47_1049-54del
ENST00000376237.8:c.*635+47_*636-54del	ENSP00000365412.4:n.*635+47_*636-54del
ENST00000383329.7:c.1066+47_1067-54del	ENSP00000372819.3:n.1066+47_1067-54del
ENST00000466892.5:n.221_228del
ENST00000470363.5:n.806+47_807-54del
ENST00000487245.5:n.1407+47_1408-54del
NM_002117.5:c.1048+47_1049-54del	NP_002108.4:n.1048+47_1049-54del
NM_002117.6:c.1048+47_1049-54del MANE Select	NP_002108.4:n.1048+47_1049-54del