Canonical Allele Identifier: CA1654354862

Gene: FOXO3

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.108574193G= , CM000668.2:g.108574193G=	GRCh38
NC_000006.11:g.108895396G= , CM000668.1:g.108895396G=	GRCh37
NC_000006.10:g.109002089G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406360.2:c.621+12364G= MANE Select	ENSP00000385824.1:n.621+12364G=
ENST00000343882.10:c.621+12364G=	ENSP00000339527.6:n.621+12364G=
ENST00000406360.1:c.621+12364G=	ENSP00000385824.1:n.621+12364G=
NM_001455.3:c.621+12364G=	NP_001446.1:n.621+12364G=
NM_201559.2:c.621+12364G=	NP_963853.1:n.621+12364G=
XM_005266867.3:c.-64+12364G=	XP_005266924.1:n.-64+12364G=
XM_011535626.1:c.120+12050G=	XP_011533928.1:n.120+12050G=
XM_005266867.4:c.-64+12364G=	XP_005266924.1:n.-64+12364G=
XM_011535626.2:c.120+12050G=	XP_011533928.1:n.120+12050G=
XM_017010585.1:c.-64+4451G=	XP_016866074.1:n.-64+4451G=
XM_017010586.1:c.-40+4451G=	XP_016866075.1:n.-40+4451G=
NM_001455.4:c.621+12364G= MANE Select	NP_001446.1:n.621+12364G=
NM_201559.3:c.621+12364G=	NP_963853.1:n.621+12364G=