Canonical Allele Identifier: CA2711332405

Gene: HLA-C

Linked Data

• dbSNP Id: rs2113902074

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269395_31269408del , CM000668.2:g.31269395_31269408del	GRCh38
NC_000006.11:g.31237172_31237185del , CM000668.1:g.31237172_31237185del	GRCh37
NC_000006.10:g.31345151_31345164del	NCBI36
NG_029422.2:g.7724_7737del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.1049-23_1049-10del MANE Select	ENSP00000365402.5:n.1049-23_1049-10del
ENST00000376228.9:c.1049-23_1049-10del	ENSP00000365402.5:n.1049-23_1049-10del
ENST00000376237.8:c.*636-23_*636-10del	ENSP00000365412.4:n.*636-23_*636-10del
ENST00000383329.7:c.1067-23_1067-10del	ENSP00000372819.3:n.1067-23_1067-10del
ENST00000466892.5:n.259_272del
ENST00000470363.5:n.807-23_807-10del
ENST00000487245.5:n.1408-23_1408-10del
NM_002117.5:c.1049-23_1049-10del	NP_002108.4:n.1049-23_1049-10del
NM_002117.6:c.1049-23_1049-10del MANE Select	NP_002108.4:n.1049-23_1049-10del