Canonical Allele Identifier: CA1654354886
Gene: FOXO3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.108574212G= , CM000668.2:g.108574212G= GRCh38
NC_000006.11:g.108895415G= , CM000668.1:g.108895415G= GRCh37
NC_000006.10:g.109002108G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000406360.2:c.621+12383G= MANE Select ENSP00000385824.1:n.621+12383G=
ENST00000343882.10:c.621+12383G= ENSP00000339527.6:n.621+12383G=
ENST00000406360.1:c.621+12383G= ENSP00000385824.1:n.621+12383G=
NM_001455.3:c.621+12383G= NP_001446.1:n.621+12383G=
NM_201559.2:c.621+12383G= NP_963853.1:n.621+12383G=
XM_005266867.3:c.-64+12383G= XP_005266924.1:n.-64+12383G=
XM_011535626.1:c.120+12069G= XP_011533928.1:n.120+12069G=
XM_005266867.4:c.-64+12383G= XP_005266924.1:n.-64+12383G=
XM_011535626.2:c.120+12069G= XP_011533928.1:n.120+12069G=
XM_017010585.1:c.-64+4470G= XP_016866074.1:n.-64+4470G=
XM_017010586.1:c.-40+4470G= XP_016866075.1:n.-40+4470G=
NM_001455.4:c.621+12383G= MANE Select NP_001446.1:n.621+12383G=
NM_201559.3:c.621+12383G= NP_963853.1:n.621+12383G=