Canonical Allele Identifier: CA2711332584

Gene: HLA-C

Linked Data

• dbSNP Id: rs2113902395

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269465_31269466insTTC , CM000668.2:g.31269465_31269466insTTC	GRCh38
NC_000006.11:g.31237242_31237243insTTC , CM000668.1:g.31237242_31237243insTTC	GRCh37
NC_000006.10:g.31345221_31345222insTTC	NCBI36
NG_029422.2:g.7668_7669insAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.1048+29_1048+30insAGA MANE Select	ENSP00000365402.5:n.1048+29_1048+30insAGA
ENST00000376228.9:c.1048+29_1048+30insAGA	ENSP00000365402.5:n.1048+29_1048+30insAGA
ENST00000376237.8:c.*635+29_*635+30insAGA	ENSP00000365412.4:n.*635+29_*635+30insAGA
ENST00000383329.7:c.1066+29_1066+30insAGA	ENSP00000372819.3:n.1066+29_1066+30insAGA
ENST00000466892.5:n.203_204insAGA
ENST00000470363.5:n.806+29_806+30insAGA
ENST00000487245.5:n.1407+29_1407+30insAGA
NM_002117.5:c.1048+29_1048+30insAGA	NP_002108.4:n.1048+29_1048+30insAGA
NM_002117.6:c.1048+29_1048+30insAGA MANE Select	NP_002108.4:n.1048+29_1048+30insAGA