Canonical Allele Identifier: CA136862054

Gene: HLA-C

Linked Data

• dbSNP Id: rs386698956

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269478_31269480delinsACT , CM000668.2:g.31269478_31269480delinsACT	GRCh38
NC_000006.11:g.31237255_31237257delinsACT , CM000668.1:g.31237255_31237257delinsACT	GRCh37
NC_000006.10:g.31345234_31345236delinsACT	NCBI36
NG_029422.2:g.7652_7654delinsAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.1048+13_1048+15delinsAGT MANE Select	ENSP00000365402.5:n.1048+13_1048+15delinsAGT
ENST00000376228.9:c.1048+13_1048+15delinsAGT	ENSP00000365402.5:n.1048+13_1048+15delinsAGT
ENST00000376237.8:c.*635+13_*635+15delinsAGT	ENSP00000365412.4:n.*635+13_*635+15delinsAGT
ENST00000383329.7:c.1066+13_1066+15delinsAGT	ENSP00000372819.3:n.1066+13_1066+15delinsAGT
ENST00000466892.5:n.187_189delinsAGT
ENST00000470363.5:n.806+13_806+15delinsAGT
ENST00000487245.5:n.1407+13_1407+15delinsAGT
NM_002117.5:c.1048+13_1048+15delinsAGT	NP_002108.4:n.1048+13_1048+15delinsAGT
NM_002117.6:c.1048+13_1048+15delinsAGT MANE Select	NP_002108.4:n.1048+13_1048+15delinsAGT