Canonical Allele Identifier: CA2677950321

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31270045-A-AGCTGGGCCAGAC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31270045_31270046insGCTGGGCCAGAC , CM000668.2:g.31270045_31270046insGCTGGGCCAGAC	GRCh38
NC_000006.11:g.31237822_31237823insGCTGGGCCAGAC , CM000668.1:g.31237822_31237823insGCTGGGCCAGAC	GRCh37
NC_000006.10:g.31345801_31345802insGCTGGGCCAGAC	NCBI36
NG_029422.2:g.7086_7087insGTCTGGCCCAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.935_936insGTCTGGCCCAGC MANE Select	ENSP00000365402.5:p.Val312_Ala313insSerGlyProAla
ENST00000376228.9:c.935_936insGTCTGGCCCAGC	ENSP00000365402.5:p.Val312_Ala313insSerGlyProAla
ENST00000376237.8:c.*522_*523insGTCTGGCCCAGC	ENSP00000365412.4:n.*522_*523insGTCTGGCCCAGC
ENST00000383329.7:c.935_936insGTCTGGCCCAGC	ENSP00000372819.3:p.Val312_Ala313insSerGlyProAla
ENST00000470363.5:n.253_254insGTCTGGCCCAGC
ENST00000487245.5:n.1294_1295insGTCTGGCCCAGC
NM_002117.5:c.935_936insGTCTGGCCCAGC	NP_002108.4:p.Val312_Ala313insSerGlyProAla
NM_002117.6:c.935_936insGTCTGGCCCAGC MANE Select	NP_002108.4:p.Val312_Ala313insSerGlyProAla