Canonical Allele Identifier: CA817003766

Gene: FOXO3

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.108682118T>A , CM000668.2:g.108682118T>A	GRCh38
NC_000006.11:g.109003321T>A , CM000668.1:g.109003321T>A	GRCh37
NC_000006.10:g.109110014T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001455.4:c.*2326T>A MANE Select	NP_001446.1:n.*2326T>A
ENST00000406360.2:c.*2326T>A MANE Select	ENSP00000385824.1:n.*2326T>A
NM_001455.3:c.*2326T>A	NP_001446.1:n.*2326T>A
NM_201559.2:c.*2326T>A	NP_963853.1:n.*2326T>A
NM_201559.3:c.*2326T>A	NP_963853.1:n.*2326T>A
ENST00000343882.10:c.*2326T>A	ENSP00000339527.6:n.*2326T>A
ENST00000406360.1:c.*2326T>A	ENSP00000385824.1:n.*2326T>A
XM_005266867.3:c.*2326T>A	XP_005266924.1:n.*2326T>A
XM_005266867.4:c.*2326T>A	XP_005266924.1:n.*2326T>A
XM_005266868.2:c.*2326T>A	XP_005266925.1:n.*2326T>A
XM_005266868.3:c.*2326T>A	XP_005266925.1:n.*2326T>A
XM_011535626.1:c.*2326T>A	XP_011533928.1:n.*2326T>A
XM_011535626.2:c.*2326T>A	XP_011533928.1:n.*2326T>A
XM_011535627.1:c.*2326T>A	XP_011533929.1:n.*2326T>A
XM_011535628.1:c.*2326T>A	XP_011533930.1:n.*2326T>A
XM_011535628.3:c.*2326T>A	XP_011533930.1:n.*2326T>A
XM_011535629.1:c.*2326T>A	XP_011533931.1:n.*2326T>A
XM_011535629.2:c.*2326T>A	XP_011533931.1:n.*2326T>A
XM_017010585.1:c.*2326T>A	XP_016866074.1:n.*2326T>A
XM_017010586.1:c.*2326T>A	XP_016866075.1:n.*2326T>A