Canonical Allele Identifier: CA2711332356

Gene: HLA-C

Linked Data

• dbSNP Id: rs2113902036

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269390_31269391insAC , CM000668.2:g.31269390_31269391insAC	GRCh38
NC_000006.11:g.31237167_31237168insAC , CM000668.1:g.31237167_31237168insAC	GRCh37
NC_000006.10:g.31345146_31345147insAC	NCBI36
NG_029422.2:g.7741_7742insGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.1049-6_1049-5insGT MANE Select	ENSP00000365402.5:n.1049-6_1049-5insGT
ENST00000376228.9:c.1049-6_1049-5insGT	ENSP00000365402.5:n.1049-6_1049-5insGT
ENST00000376237.8:c.*636-6_*636-5insGT	ENSP00000365412.4:n.*636-6_*636-5insGT
ENST00000383329.7:c.1067-6_1067-5insGT	ENSP00000372819.3:n.1067-6_1067-5insGT
ENST00000466892.5:n.276_277insGT
ENST00000470363.5:n.807-6_807-5insGT
ENST00000487245.5:n.1408-6_1408-5insGT
NM_002117.5:c.1049-6_1049-5insGT	NP_002108.4:n.1049-6_1049-5insGT
NM_002117.6:c.1049-6_1049-5insGT MANE Select	NP_002108.4:n.1049-6_1049-5insGT