Canonical Allele Identifier: CA1619080105
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270712_31270714delinsCTG , CM000668.2:g.31270712_31270714delinsCTG GRCh38
NC_000006.11:g.31238489_31238491delinsCTG , CM000668.1:g.31238489_31238491delinsCTG GRCh37
NC_000006.10:g.31346468_31346470delinsCTG NCBI36
NG_029422.2:g.6418_6420delinsCAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.620-229_620-227delinsCAG MANE Select ENSP00000365402.5:n.620-229_620-227delinsCAG
ENST00000376228.9:c.620-229_620-227delinsCAG ENSP00000365402.5:n.620-229_620-227delinsCAG
ENST00000376237.8:c.*207-229_*207-227delinsCAG ENSP00000365412.4:n.*207-229_*207-227delinsCAG
ENST00000383329.7:c.620-229_620-227delinsCAG ENSP00000372819.3:n.620-229_620-227delinsCAG
ENST00000415537.1:c.618-229_618-227delinsCAG
ENST00000487245.5:n.979-229_979-227delinsCAG
ENST00000495835.1:n.809-229_809-227delinsCAG
NM_002117.5:c.620-229_620-227delinsCAG NP_002108.4:n.620-229_620-227delinsCAG
NM_002117.6:c.620-229_620-227delinsCAG MANE Select NP_002108.4:n.620-229_620-227delinsCAG