Canonical Allele Identifier: CA1654345800
Gene: FOXO3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.108567390C= , CM000668.2:g.108567390C= GRCh38
NC_000006.11:g.108888593C= , CM000668.1:g.108888593C= GRCh37
NC_000006.10:g.108995286C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001455.4:c.621+5561C= MANE Select NP_001446.1:n.621+5561C=
ENST00000406360.2:c.621+5561C= MANE Select ENSP00000385824.1:n.621+5561C=
NM_001455.3:c.621+5561C= NP_001446.1:n.621+5561C=
NM_201559.2:c.621+5561C= NP_963853.1:n.621+5561C=
NM_201559.3:c.621+5561C= NP_963853.1:n.621+5561C=
ENST00000343882.10:c.621+5561C= ENSP00000339527.6:n.621+5561C=
ENST00000406360.1:c.621+5561C= ENSP00000385824.1:n.621+5561C=
XM_005266867.3:c.-64+5561C= XP_005266924.1:n.-64+5561C=
XM_005266867.4:c.-64+5561C= XP_005266924.1:n.-64+5561C=
XM_011535626.1:c.120+5247C= XP_011533928.1:n.120+5247C=
XM_011535626.2:c.120+5247C= XP_011533928.1:n.120+5247C=