Canonical Allele Identifier: CA1654428001

Gene: FOXO3

Linked Data

• dbSNP Id: rs1770668578

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.108677690_108677691del , CM000668.2:g.108677690_108677691del	GRCh38
NC_000006.11:g.108998893_108998894del , CM000668.1:g.108998893_108998894del	GRCh37
NC_000006.10:g.109105586_109105587del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000406360.2:c.*35-2137_*35-2136del MANE Select	ENSP00000385824.1:n.*35-2137_*35-2136del
ENST00000343882.10:c.*35-2137_*35-2136del	ENSP00000339527.6:n.*35-2137_*35-2136del
ENST00000406360.1:c.*35-2137_*35-2136del	ENSP00000385824.1:n.*35-2137_*35-2136del
ENST00000540898.1:c.*35-2137_*35-2136del	ENSP00000446316.1:n.*35-2137_*35-2136del
NM_001455.3:c.*35-2137_*35-2136del	NP_001446.1:n.*35-2137_*35-2136del
NM_201559.2:c.*35-2137_*35-2136del	NP_963853.1:n.*35-2137_*35-2136del
XM_005266867.3:c.*35-2137_*35-2136del	XP_005266924.1:n.*35-2137_*35-2136del
XM_005266868.2:c.*35-2137_*35-2136del	XP_005266925.1:n.*35-2137_*35-2136del
XM_011535626.1:c.*35-2137_*35-2136del	XP_011533928.1:n.*35-2137_*35-2136del
XM_011535627.1:c.*35-2137_*35-2136del	XP_011533929.1:n.*35-2137_*35-2136del
XM_011535628.1:c.*35-2137_*35-2136del	XP_011533930.1:n.*35-2137_*35-2136del
XM_011535629.1:c.*35-2137_*35-2136del	XP_011533931.1:n.*35-2137_*35-2136del
XM_005266867.4:c.*35-2137_*35-2136del	XP_005266924.1:n.*35-2137_*35-2136del
XM_005266868.3:c.*35-2137_*35-2136del	XP_005266925.1:n.*35-2137_*35-2136del
XM_011535626.2:c.*35-2137_*35-2136del	XP_011533928.1:n.*35-2137_*35-2136del
XM_011535628.3:c.*35-2137_*35-2136del	XP_011533930.1:n.*35-2137_*35-2136del
XM_011535629.2:c.*35-2137_*35-2136del	XP_011533931.1:n.*35-2137_*35-2136del
XM_017010585.1:c.*35-2137_*35-2136del	XP_016866074.1:n.*35-2137_*35-2136del
XM_017010586.1:c.*35-2137_*35-2136del	XP_016866075.1:n.*35-2137_*35-2136del
NM_001455.4:c.*35-2137_*35-2136del MANE Select	NP_001446.1:n.*35-2137_*35-2136del
NM_201559.3:c.*35-2137_*35-2136del	NP_963853.1:n.*35-2137_*35-2136del