Canonical Allele Identifier: CA1654392080

Gene: FOXO3

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.108656460T>G , CM000668.2:g.108656460T>G	GRCh38
NC_000006.11:g.108977663T>G , CM000668.1:g.108977663T>G	GRCh37
NC_000006.10:g.109084356T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001455.4:c.622-6995T>G MANE Select	NP_001446.1:n.622-6995T>G
ENST00000406360.2:c.622-6995T>G MANE Select	ENSP00000385824.1:n.622-6995T>G
NM_001455.3:c.622-6995T>G	NP_001446.1:n.622-6995T>G
NM_201559.2:c.622-6995T>G	NP_963853.1:n.622-6995T>G
NM_201559.3:c.622-6995T>G	NP_963853.1:n.622-6995T>G
ENST00000343882.10:c.622-6995T>G	ENSP00000339527.6:n.622-6995T>G
ENST00000406360.1:c.622-6995T>G	ENSP00000385824.1:n.622-6995T>G
ENST00000540898.1:c.-118T>G	ENSP00000446316.1:n.-118T>G
XM_005266867.3:c.55-6995T>G	XP_005266924.1:n.55-6995T>G
XM_005266867.4:c.55-6995T>G	XP_005266924.1:n.55-6995T>G
XM_005266868.2:c.-118T>G	XP_005266925.1:n.-118T>G
XM_005266868.3:c.-118T>G	XP_005266925.1:n.-118T>G
XM_011535626.1:c.121-6995T>G	XP_011533928.1:n.121-6995T>G
XM_011535626.2:c.121-6995T>G	XP_011533928.1:n.121-6995T>G
XM_011535627.1:c.70-6995T>G	XP_011533929.1:n.70-6995T>G
XM_011535628.1:c.-39-6995T>G	XP_011533930.1:n.-39-6995T>G
XM_011535628.3:c.-39-6995T>G	XP_011533930.1:n.-39-6995T>G
XM_011535629.1:c.-40+95T>G	XP_011533931.1:n.-40+95T>G
XM_011535629.2:c.-40+95T>G	XP_011533931.1:n.-40+95T>G
XM_017010585.1:c.55-6995T>G	XP_016866074.1:n.55-6995T>G
XM_017010586.1:c.-39-6995T>G	XP_016866075.1:n.-39-6995T>G