Canonical Allele Identifier: CA136865890

Gene: HLA-C

Linked Data

• dbSNP Id: rs796887986

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31270453_31270457delinsCGAGA , CM000668.2:g.31270453_31270457delinsCGAGA	GRCh38
NC_000006.11:g.31238230_31238234delinsCGAGA , CM000668.1:g.31238230_31238234delinsCGAGA	GRCh37
NC_000006.10:g.31346209_31346213delinsCGAGA	NCBI36
NG_029422.2:g.6675_6679delinsTCTCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.648_652delinsTCTCG MANE Select	ENSP00000365402.5:p.Pro217_Leu218delinsLeuVal
ENST00000376228.9:c.648_652delinsTCTCG	ENSP00000365402.5:p.Pro217_Leu218delinsLeuVal
ENST00000376237.8:c.*235_*239delinsTCTCG	ENSP00000365412.4:n.*235_*239delinsTCTCG
ENST00000383329.7:c.648_652delinsTCTCG	ENSP00000372819.3:p.Pro217_Leu218delinsLeuVal
ENST00000415537.1:c.646_650delinsTCTCG
ENST00000487245.5:n.1007_1011delinsTCTCG
ENST00000495835.1:n.837_841delinsTCTCG
NM_002117.5:c.648_652delinsTCTCG	NP_002108.4:p.Pro217_Leu218delinsLeuVal
NM_002117.6:c.648_652delinsTCTCG MANE Select	NP_002108.4:p.Pro217_Leu218delinsLeuVal