Canonical Allele Identifier: CA1619077344
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269122_31269123delinsAG , CM000668.2:g.31269122_31269123delinsAG GRCh38
NC_000006.11:g.31236899_31236900delinsAG , CM000668.1:g.31236899_31236900delinsAG GRCh37
NC_000006.10:g.31344878_31344879delinsAG NCBI36
NG_029422.2:g.8009_8010delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.*46_*47delinsCT MANE Select ENSP00000365402.5:n.*46_*47delinsCT
ENST00000376228.9:c.*46_*47delinsCT ENSP00000365402.5:n.*46_*47delinsCT
ENST00000376237.8:c.*734_*735delinsCT ENSP00000365412.4:n.*734_*735delinsCT
ENST00000383329.7:c.*46_*47delinsCT ENSP00000372819.3:n.*46_*47delinsCT
ENST00000466892.5:n.380_381delinsCT
ENST00000470363.5:n.905_906delinsCT
ENST00000487245.5:n.1506_1507delinsCT
NM_002117.5:c.*46_*47delinsCT NP_002108.4:n.*46_*47delinsCT
NM_002117.6:c.*46_*47delinsCT MANE Select NP_002108.4:n.*46_*47delinsCT