Canonical Allele Identifier: CA12435945

Gene: FOXO3

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.108613258C>T , CM000668.2:g.108613258C>T	GRCh38
NC_000006.11:g.108934461C>T , CM000668.1:g.108934461C>T	GRCh37
NC_000006.10:g.109041154C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406360.2:c.622-50197C>T MANE Select	ENSP00000385824.1:n.622-50197C>T
ENST00000343882.10:c.622-50197C>T	ENSP00000339527.6:n.622-50197C>T
ENST00000406360.1:c.622-50197C>T	ENSP00000385824.1:n.622-50197C>T
NM_001455.3:c.622-50197C>T	NP_001446.1:n.622-50197C>T
NM_201559.2:c.622-50197C>T	NP_963853.1:n.622-50197C>T
XM_005266867.3:c.-63-26235C>T	XP_005266924.1:n.-63-26235C>T
XM_011535626.1:c.121-50197C>T	XP_011533928.1:n.121-50197C>T
XM_011535627.1:c.69+26622C>T	XP_011533929.1:n.69+26622C>T
XM_011535628.1:c.-40+23443C>T	XP_011533930.1:n.-40+23443C>T
XM_005266867.4:c.-63-26235C>T	XP_005266924.1:n.-63-26235C>T
XM_011535626.2:c.121-50197C>T	XP_011533928.1:n.121-50197C>T
XM_011535628.3:c.-40+23443C>T	XP_011533930.1:n.-40+23443C>T
XM_017010585.1:c.-63-26235C>T	XP_016866074.1:n.-63-26235C>T
XM_017010586.1:c.-40+43516C>T	XP_016866075.1:n.-40+43516C>T
NM_001455.4:c.622-50197C>T MANE Select	NP_001446.1:n.622-50197C>T
NM_201559.3:c.622-50197C>T	NP_963853.1:n.622-50197C>T