Canonical Allele Identifier: CA1654354853

Gene: FOXO3

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.108574190C= , CM000668.2:g.108574190C=	GRCh38
NC_000006.11:g.108895393C= , CM000668.1:g.108895393C=	GRCh37
NC_000006.10:g.109002086C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000406360.2:c.621+12361C= MANE Select	ENSP00000385824.1:n.621+12361C=
ENST00000343882.10:c.621+12361C=	ENSP00000339527.6:n.621+12361C=
ENST00000406360.1:c.621+12361C=	ENSP00000385824.1:n.621+12361C=
NM_001455.3:c.621+12361C=	NP_001446.1:n.621+12361C=
NM_201559.2:c.621+12361C=	NP_963853.1:n.621+12361C=
XM_005266867.3:c.-64+12361C=	XP_005266924.1:n.-64+12361C=
XM_011535626.1:c.120+12047C=	XP_011533928.1:n.120+12047C=
XM_005266867.4:c.-64+12361C=	XP_005266924.1:n.-64+12361C=
XM_011535626.2:c.120+12047C=	XP_011533928.1:n.120+12047C=
XM_017010585.1:c.-64+4448C=	XP_016866074.1:n.-64+4448C=
XM_017010586.1:c.-40+4448C=	XP_016866075.1:n.-40+4448C=
NM_001455.4:c.621+12361C= MANE Select	NP_001446.1:n.621+12361C=
NM_201559.3:c.621+12361C=	NP_963853.1:n.621+12361C=