Canonical Allele Identifier: CA2711332407

Gene: HLA-C

Linked Data

• dbSNP Id: rs2113902146

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269413_31269415del , CM000668.2:g.31269413_31269415del	GRCh38
NC_000006.11:g.31237190_31237192del , CM000668.1:g.31237190_31237192del	GRCh37
NC_000006.10:g.31345169_31345171del	NCBI36
NG_029422.2:g.7717_7719del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.1049-30_1049-28del MANE Select	ENSP00000365402.5:n.1049-30_1049-28del
ENST00000376228.9:c.1049-30_1049-28del	ENSP00000365402.5:n.1049-30_1049-28del
ENST00000376237.8:c.*636-30_*636-28del	ENSP00000365412.4:n.*636-30_*636-28del
ENST00000383329.7:c.1067-30_1067-28del	ENSP00000372819.3:n.1067-30_1067-28del
ENST00000466892.5:n.252_254del
ENST00000470363.5:n.807-30_807-28del
ENST00000487245.5:n.1408-30_1408-28del
NM_002117.5:c.1049-30_1049-28del	NP_002108.4:n.1049-30_1049-28del
NM_002117.6:c.1049-30_1049-28del MANE Select	NP_002108.4:n.1049-30_1049-28del