Canonical Allele Identifier: CA365339493
Gene: FOXO3 HGNC NCBI

Linked Data

ClinVar Variation Id: 438764
ClinVar RCV Id: RCV000505635
dbSNP Id: rs1554218944

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.108663532G>A , CM000668.2:g.108663532G>A GRCh38
NC_000006.11:g.108984735G>A , CM000668.1:g.108984735G>A GRCh37
NC_000006.10:g.109091428G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000406360.2:c.699G>A MANE Select ENSP00000385824.1:p.Trp233Ter
ENST00000343882.10:c.699G>A ENSP00000339527.6:p.Trp233Ter
ENST00000406360.1:c.699G>A ENSP00000385824.1:p.Trp233Ter
ENST00000540898.1:c.39G>A ENSP00000446316.1:p.Trp13Ter
NM_001455.3:c.699G>A NP_001446.1:p.Trp233Ter
NM_201559.2:c.699G>A NP_963853.1:p.Trp233Ter
XM_005266867.3:c.132G>A XP_005266924.1:p.Trp44Ter
XM_005266868.2:c.39G>A XP_005266925.1:p.Trp13Ter
XM_011535626.1:c.198G>A XP_011533928.1:p.Trp66Ter
XM_011535627.1:c.147G>A XP_011533929.1:p.Trp49Ter
XM_011535628.1:c.39G>A XP_011533930.1:p.Trp13Ter
XM_011535629.1:c.39G>A XP_011533931.1:p.Trp13Ter
XM_005266867.4:c.132G>A XP_005266924.1:p.Trp44Ter
XM_005266868.3:c.39G>A XP_005266925.1:p.Trp13Ter
XM_011535626.2:c.198G>A XP_011533928.1:p.Trp66Ter
XM_011535628.3:c.39G>A XP_011533930.1:p.Trp13Ter
XM_011535629.2:c.39G>A XP_011533931.1:p.Trp13Ter
XM_017010585.1:c.132G>A XP_016866074.1:p.Trp44Ter
XM_017010586.1:c.39G>A XP_016866075.1:p.Trp13Ter
NM_001455.4:c.699G>A MANE Select NP_001446.1:p.Trp233Ter
NM_201559.3:c.699G>A NP_963853.1:p.Trp233Ter