Canonical Allele Identifier: CA2711332891

Gene: HLA-C

Linked Data

• dbSNP Id: rs2113902680

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269521_31269522insAGGACAGCTAGGACAG , CM000668.2:g.31269521_31269522insAGGACAGCTAGGACAG	GRCh38
NC_000006.11:g.31237298_31237299insAGGACAGCTAGGACAG , CM000668.1:g.31237298_31237299insAGGACAGCTAGGACAG	GRCh37
NC_000006.10:g.31345277_31345278insAGGACAGCTAGGACAG	NCBI36
NG_029422.2:g.7610_7611insCTGTCCTAGCTGTCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.1019_1020insCTGTCCTAGCTGTCCT MANE Select	ENSP00000365402.5:p.Lys341CysfsTer23
ENST00000376228.9:c.1019_1020insCTGTCCTAGCTGTCCT	ENSP00000365402.5:p.Lys341CysfsTer23
ENST00000376237.8:c.*606_*607insCTGTCCTAGCTGTCCT	ENSP00000365412.4:n.*606_*607insCTGTCCTAGCTGTCCT
ENST00000383329.7:c.1037_1038insCTGTCCTAGCTGTCCT	ENSP00000372819.3:p.Lys347CysfsTer23
ENST00000466892.5:n.145_146insCTGTCCTAGCTGTCCT
ENST00000470363.5:n.777_778insCTGTCCTAGCTGTCCT
ENST00000487245.5:n.1378_1379insCTGTCCTAGCTGTCCT
NM_002117.5:c.1019_1020insCTGTCCTAGCTGTCCT	NP_002108.4:p.Lys341CysfsTer23
NM_002117.6:c.1019_1020insCTGTCCTAGCTGTCCT MANE Select	NP_002108.4:p.Lys341CysfsTer23