Canonical Allele Identifier: CA2679911225
Gene: FOXO3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.108561766_108561781del , CM000668.2:g.108561766_108561781del GRCh38
NC_000006.11:g.108882969_108882984del , CM000668.1:g.108882969_108882984del GRCh37
NC_000006.10:g.108989662_108989677del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000406360.2:c.558_573del MANE Select ENSP00000385824.1:p.Trp186CysfsTer?
ENST00000343882.10:c.558_573del ENSP00000339527.6:p.Trp186CysfsTer?
ENST00000406360.1:c.558_573del ENSP00000385824.1:p.Trp186CysfsTer?
NM_001455.3:c.558_573del NP_001446.1:p.Trp186CysfsTer?
NM_201559.2:c.558_573del NP_963853.1:p.Trp186CysfsTer?
XM_005266867.3:c.-127_-112del XP_005266924.1:n.-127_-112del
XM_005266867.4:c.-127_-112del XP_005266924.1:n.-127_-112del
NM_001455.4:c.558_573del MANE Select NP_001446.1:p.Trp186CysfsTer?
NM_201559.3:c.558_573del NP_963853.1:p.Trp186CysfsTer?