Canonical Allele Identifier: CA145713656

Gene: FOXO3

Linked Data

• dbSNP Id: rs887114132
• gnomAD v2: 6-108895412-G-GT
• gnomAD v3: 6-108574209-G-GT
• gnomAD v4: 6-108574209-G-GT
• MyVariant Identifiers: chr6:g.108895412_108895413insT (hg19) ; chr6:g.108574209_108574210insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.108574210dup , CM000668.2:g.108574210dup	GRCh38
NC_000006.11:g.108895413dup , CM000668.1:g.108895413dup	GRCh37
NC_000006.10:g.109002106dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406360.2:c.621+12381dup MANE Select	ENSP00000385824.1:n.621+12381dup
ENST00000343882.10:c.621+12381dup	ENSP00000339527.6:n.621+12381dup
ENST00000406360.1:c.621+12381dup	ENSP00000385824.1:n.621+12381dup
NM_001455.3:c.621+12381dup	NP_001446.1:n.621+12381dup
NM_201559.2:c.621+12381dup	NP_963853.1:n.621+12381dup
XM_005266867.3:c.-64+12381dup	XP_005266924.1:n.-64+12381dup
XM_011535626.1:c.120+12067dup	XP_011533928.1:n.120+12067dup
XM_005266867.4:c.-64+12381dup	XP_005266924.1:n.-64+12381dup
XM_011535626.2:c.120+12067dup	XP_011533928.1:n.120+12067dup
XM_017010585.1:c.-64+4468dup	XP_016866074.1:n.-64+4468dup
XM_017010586.1:c.-40+4468dup	XP_016866075.1:n.-40+4468dup
NM_001455.4:c.621+12381dup MANE Select	NP_001446.1:n.621+12381dup
NM_201559.3:c.621+12381dup	NP_963853.1:n.621+12381dup