Canonical Allele Identifier: CA136865890
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs796887986
JSON-LD

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
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