Canonical Allele Identifier: CA2677950298

Gene: HLA-C

Linked Data - Sequence & Population

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269999_31270000insAGCCAT , CM000668.2:g.31269999_31270000insAGCCAT	GRCh38
NC_000006.11:g.31237776_31237777insAGCCAT , CM000668.1:g.31237776_31237777insAGCCAT	GRCh37
NC_000006.10:g.31345755_31345756insAGCCAT	NCBI36
NG_029422.2:g.7132_7133insATGGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.981_982insATGGCT MANE Select	ENSP00000365402.5:p.Val327_Val328insMetAla
ENST00000376228.9:c.981_982insATGGCT	ENSP00000365402.5:p.Val327_Val328insMetAla
ENST00000376237.8:c.*568_*569insATGGCT	ENSP00000365412.4:n.*568_*569insATGGCT
ENST00000383329.7:c.981_982insATGGCT	ENSP00000372819.3:p.Val327_Val328insMetAla
ENST00000470363.5:n.299_300insATGGCT
ENST00000487245.5:n.1340_1341insATGGCT
NM_002117.5:c.981_982insATGGCT	NP_002108.4:p.Val327_Val328insMetAla
NM_002117.6:c.981_982insATGGCT MANE Select	NP_002108.4:p.Val327_Val328insMetAla