Canonical Allele Identifier: CA2711332824

Gene: HLA-C

Linked Data

• dbSNP Id: rs2113902542

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269492del , CM000668.2:g.31269492del	GRCh38
NC_000006.11:g.31237269del , CM000668.1:g.31237269del	GRCh37
NC_000006.10:g.31345248del	NCBI36
NG_029422.2:g.7640del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.1048+1del MANE Select	ENSP00000365402.5:n.1048+1del
ENST00000376228.9:c.1048+1del	ENSP00000365402.5:n.1048+1del
ENST00000376237.8:c.*635+1del	ENSP00000365412.4:n.*635+1del
ENST00000383329.7:c.1066+1del	ENSP00000372819.3:n.1066+1del
ENST00000466892.5:n.175del
ENST00000470363.5:n.806+1del
ENST00000487245.5:n.1407+1del
NM_002117.5:c.1048+1del	NP_002108.4:n.1048+1del
NM_002117.6:c.1048+1del MANE Select	NP_002108.4:n.1048+1del