Canonical Allele Identifier: CA2711332692

Gene: HLA-C

Linked Data

• dbSNP Id: rs2113902528

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269489_31269490del , CM000668.2:g.31269489_31269490del	GRCh38
NC_000006.11:g.31237266_31237267del , CM000668.1:g.31237266_31237267del	GRCh37
NC_000006.10:g.31345245_31345246del	NCBI36
NG_029422.2:g.7642_7643del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.1048+3_1048+4del MANE Select	ENSP00000365402.5:n.1048+3_1048+4del
ENST00000376228.9:c.1048+3_1048+4del	ENSP00000365402.5:n.1048+3_1048+4del
ENST00000376237.8:c.*635+3_*635+4del	ENSP00000365412.4:n.*635+3_*635+4del
ENST00000383329.7:c.1066+3_1066+4del	ENSP00000372819.3:n.1066+3_1066+4del
ENST00000466892.5:n.177_178del
ENST00000470363.5:n.806+3_806+4del
ENST00000487245.5:n.1407+3_1407+4del
NM_002117.5:c.1048+3_1048+4del	NP_002108.4:n.1048+3_1048+4del
NM_002117.6:c.1048+3_1048+4del MANE Select	NP_002108.4:n.1048+3_1048+4del