Canonical Allele Identifier: CA1654376219

Gene: FOXO3

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.108595370T= , CM000668.2:g.108595370T=	GRCh38
NC_000006.11:g.108916573T= , CM000668.1:g.108916573T=	GRCh37
NC_000006.10:g.109023266T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001455.4:c.621+33541T= MANE Select	NP_001446.1:n.621+33541T=
ENST00000406360.2:c.621+33541T= MANE Select	ENSP00000385824.1:n.621+33541T=
NM_001455.3:c.621+33541T=	NP_001446.1:n.621+33541T=
NM_201559.2:c.621+33541T=	NP_963853.1:n.621+33541T=
NM_201559.3:c.621+33541T=	NP_963853.1:n.621+33541T=
ENST00000343882.10:c.621+33541T=	ENSP00000339527.6:n.621+33541T=
ENST00000406360.1:c.621+33541T=	ENSP00000385824.1:n.621+33541T=
XM_005266867.3:c.-64+33541T=	XP_005266924.1:n.-64+33541T=
XM_005266867.4:c.-64+33541T=	XP_005266924.1:n.-64+33541T=
XM_011535626.1:c.120+33227T=	XP_011533928.1:n.120+33227T=
XM_011535626.2:c.120+33227T=	XP_011533928.1:n.120+33227T=
XM_011535627.1:c.69+8734T=	XP_011533929.1:n.69+8734T=
XM_011535628.1:c.-40+5555T=	XP_011533930.1:n.-40+5555T=
XM_011535628.3:c.-40+5555T=	XP_011533930.1:n.-40+5555T=
XM_017010585.1:c.-64+25628T=	XP_016866074.1:n.-64+25628T=
XM_017010586.1:c.-40+25628T=	XP_016866075.1:n.-40+25628T=