Canonical Allele Identifier: CA2711332458

Gene: HLA-C

Linked Data

• dbSNP Id: rs2113902192

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269425_31269437del , CM000668.2:g.31269425_31269437del	GRCh38
NC_000006.11:g.31237202_31237214del , CM000668.1:g.31237202_31237214del	GRCh37
NC_000006.10:g.31345181_31345193del	NCBI36
NG_029422.2:g.7695_7707del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.1049-52_1049-40del MANE Select	ENSP00000365402.5:n.1049-52_1049-40del
ENST00000376228.9:c.1049-52_1049-40del	ENSP00000365402.5:n.1049-52_1049-40del
ENST00000376237.8:c.*636-52_*636-40del	ENSP00000365412.4:n.*636-52_*636-40del
ENST00000383329.7:c.1067-52_1067-40del	ENSP00000372819.3:n.1067-52_1067-40del
ENST00000466892.5:n.230_242del
ENST00000470363.5:n.807-52_807-40del
ENST00000487245.5:n.1408-52_1408-40del
NM_002117.5:c.1049-52_1049-40del	NP_002108.4:n.1049-52_1049-40del
NM_002117.6:c.1049-52_1049-40del MANE Select	NP_002108.4:n.1049-52_1049-40del