Canonical Allele Identifier: CA136861304
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs386698953

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269076_31269077delinsAC , CM000668.2:g.31269076_31269077delinsAC GRCh38
NC_000006.11:g.31236853_31236854delinsAC , CM000668.1:g.31236853_31236854delinsAC GRCh37
NC_000006.10:g.31344832_31344833delinsAC NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.*92_*93delinsGT MANE Select ENSP00000365402.5:n.*92_*93delinsGT
ENST00000376228.9:c.*92_*93delinsGT ENSP00000365402.5:n.*92_*93delinsGT
ENST00000376237.8:c.*780_*781delinsGT ENSP00000365412.4:n.*780_*781delinsGT
ENST00000383329.7:c.*92_*93delinsGT ENSP00000372819.3:n.*92_*93delinsGT
ENST00000466892.5:n.426_427delinsGT
ENST00000470363.5:n.951_952delinsGT
ENST00000487245.5:n.1552_1553delinsGT
NM_002117.5:c.*92_*93delinsGT NP_002108.4:n.*92_*93delinsGT
NM_002117.6:c.*92_*93delinsGT MANE Select NP_002108.4:n.*92_*93delinsGT