Canonical Allele Identifier: CA2711332605

Gene: HLA-C

Linked Data

• dbSNP Id: rs2113902441

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269474_31269483del , CM000668.2:g.31269474_31269483del	GRCh38
NC_000006.11:g.31237251_31237260del , CM000668.1:g.31237251_31237260del	GRCh37
NC_000006.10:g.31345230_31345239del	NCBI36
NG_029422.2:g.7650_7659del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.1048+11_1048+20del MANE Select	ENSP00000365402.5:n.1048+11_1048+20del
ENST00000376228.9:c.1048+11_1048+20del	ENSP00000365402.5:n.1048+11_1048+20del
ENST00000376237.8:c.*635+11_*635+20del	ENSP00000365412.4:n.*635+11_*635+20del
ENST00000383329.7:c.1066+11_1066+20del	ENSP00000372819.3:n.1066+11_1066+20del
ENST00000466892.5:n.185_194del
ENST00000470363.5:n.806+11_806+20del
ENST00000487245.5:n.1407+11_1407+20del
NM_002117.5:c.1048+11_1048+20del	NP_002108.4:n.1048+11_1048+20del
NM_002117.6:c.1048+11_1048+20del MANE Select	NP_002108.4:n.1048+11_1048+20del