Canonical Allele Identifier: CA2679911234

Gene: FOXO3

Linked Data

• gnomAD v4: 6-108561844-C-CGGGCTGGCAGCA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.108561847_108561858dup , CM000668.2:g.108561847_108561858dup	GRCh38
NC_000006.11:g.108883050_108883061dup , CM000668.1:g.108883050_108883061dup	GRCh37
NC_000006.10:g.108989743_108989754dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406360.2:c.621+18_621+29dup MANE Select	ENSP00000385824.1:n.621+18_621+29dup
ENST00000343882.10:c.621+18_621+29dup	ENSP00000339527.6:n.621+18_621+29dup
ENST00000406360.1:c.621+18_621+29dup	ENSP00000385824.1:n.621+18_621+29dup
NM_001455.3:c.621+18_621+29dup	NP_001446.1:n.621+18_621+29dup
NM_201559.2:c.621+18_621+29dup	NP_963853.1:n.621+18_621+29dup
XM_005266867.3:c.-64+18_-64+29dup	XP_005266924.1:n.-64+18_-64+29dup
XM_005266867.4:c.-64+18_-64+29dup	XP_005266924.1:n.-64+18_-64+29dup
NM_001455.4:c.621+18_621+29dup MANE Select	NP_001446.1:n.621+18_621+29dup
NM_201559.3:c.621+18_621+29dup	NP_963853.1:n.621+18_621+29dup