Canonical Allele Identifier: CA1654338701
Gene: FOXO3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.108561858G= , CM000668.2:g.108561858G= GRCh38
NC_000006.11:g.108883061G= , CM000668.1:g.108883061G= GRCh37
NC_000006.10:g.108989754G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000406360.2:c.621+29G= MANE Select ENSP00000385824.1:n.621+29G=
ENST00000343882.10:c.621+29G= ENSP00000339527.6:n.621+29G=
ENST00000406360.1:c.621+29G= ENSP00000385824.1:n.621+29G=
NM_001455.3:c.621+29G= NP_001446.1:n.621+29G=
NM_201559.2:c.621+29G= NP_963853.1:n.621+29G=
XM_005266867.3:c.-64+29G= XP_005266924.1:n.-64+29G=
XM_005266867.4:c.-64+29G= XP_005266924.1:n.-64+29G=
NM_001455.4:c.621+29G= MANE Select NP_001446.1:n.621+29G=
NM_201559.3:c.621+29G= NP_963853.1:n.621+29G=
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