Canonical Allele Identifier: CA1654354871
Gene: FOXO3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.108574201A= , CM000668.2:g.108574201A= GRCh38
NC_000006.11:g.108895404A= , CM000668.1:g.108895404A= GRCh37
NC_000006.10:g.109002097A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000406360.2:c.621+12372A= MANE Select ENSP00000385824.1:n.621+12372A=
ENST00000343882.10:c.621+12372A= ENSP00000339527.6:n.621+12372A=
ENST00000406360.1:c.621+12372A= ENSP00000385824.1:n.621+12372A=
NM_001455.3:c.621+12372A= NP_001446.1:n.621+12372A=
NM_201559.2:c.621+12372A= NP_963853.1:n.621+12372A=
XM_005266867.3:c.-64+12372A= XP_005266924.1:n.-64+12372A=
XM_011535626.1:c.120+12058A= XP_011533928.1:n.120+12058A=
XM_005266867.4:c.-64+12372A= XP_005266924.1:n.-64+12372A=
XM_011535626.2:c.120+12058A= XP_011533928.1:n.120+12058A=
XM_017010585.1:c.-64+4459A= XP_016866074.1:n.-64+4459A=
XM_017010586.1:c.-40+4459A= XP_016866075.1:n.-40+4459A=
NM_001455.4:c.621+12372A= MANE Select NP_001446.1:n.621+12372A=
NM_201559.3:c.621+12372A= NP_963853.1:n.621+12372A=