Canonical Allele Identifier: CA1092983150

Gene: FOXO3

Linked Data

• dbSNP Id: rs1776197315
• gnomAD v3: 6-108574184-G-GC
• gnomAD v4: 6-108574184-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.108574185dup , CM000668.2:g.108574185dup	GRCh38
NC_000006.11:g.108895388dup , CM000668.1:g.108895388dup	GRCh37
NC_000006.10:g.109002081dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000406360.2:c.621+12356dup MANE Select	ENSP00000385824.1:n.621+12356dup
ENST00000343882.10:c.621+12356dup	ENSP00000339527.6:n.621+12356dup
ENST00000406360.1:c.621+12356dup	ENSP00000385824.1:n.621+12356dup
NM_001455.3:c.621+12356dup	NP_001446.1:n.621+12356dup
NM_201559.2:c.621+12356dup	NP_963853.1:n.621+12356dup
XM_005266867.3:c.-64+12356dup	XP_005266924.1:n.-64+12356dup
XM_011535626.1:c.120+12042dup	XP_011533928.1:n.120+12042dup
XM_005266867.4:c.-64+12356dup	XP_005266924.1:n.-64+12356dup
XM_011535626.2:c.120+12042dup	XP_011533928.1:n.120+12042dup
XM_017010585.1:c.-64+4443dup	XP_016866074.1:n.-64+4443dup
XM_017010586.1:c.-40+4443dup	XP_016866075.1:n.-40+4443dup
NM_001455.4:c.621+12356dup MANE Select	NP_001446.1:n.621+12356dup
NM_201559.3:c.621+12356dup	NP_963853.1:n.621+12356dup