Canonical Allele Identifier: CA1654427952
Gene: FOXO3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.108677654G= , CM000668.2:g.108677654G= GRCh38
NC_000006.11:g.108998857G= , CM000668.1:g.108998857G= GRCh37
NC_000006.10:g.109105550G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000406360.2:c.*35-2173G= MANE Select ENSP00000385824.1:n.*35-2173G=
ENST00000343882.10:c.*35-2173G= ENSP00000339527.6:n.*35-2173G=
ENST00000406360.1:c.*35-2173G= ENSP00000385824.1:n.*35-2173G=
ENST00000540898.1:c.*35-2173G= ENSP00000446316.1:n.*35-2173G=
NM_001455.3:c.*35-2173G= NP_001446.1:n.*35-2173G=
NM_201559.2:c.*35-2173G= NP_963853.1:n.*35-2173G=
XM_005266867.3:c.*35-2173G= XP_005266924.1:n.*35-2173G=
XM_005266868.2:c.*35-2173G= XP_005266925.1:n.*35-2173G=
XM_011535626.1:c.*35-2173G= XP_011533928.1:n.*35-2173G=
XM_011535627.1:c.*35-2173G= XP_011533929.1:n.*35-2173G=
XM_011535628.1:c.*35-2173G= XP_011533930.1:n.*35-2173G=
XM_011535629.1:c.*35-2173G= XP_011533931.1:n.*35-2173G=
XM_005266867.4:c.*35-2173G= XP_005266924.1:n.*35-2173G=
XM_005266868.3:c.*35-2173G= XP_005266925.1:n.*35-2173G=
XM_011535626.2:c.*35-2173G= XP_011533928.1:n.*35-2173G=
XM_011535628.3:c.*35-2173G= XP_011533930.1:n.*35-2173G=
XM_011535629.2:c.*35-2173G= XP_011533931.1:n.*35-2173G=
XM_017010585.1:c.*35-2173G= XP_016866074.1:n.*35-2173G=
XM_017010586.1:c.*35-2173G= XP_016866075.1:n.*35-2173G=
NM_001455.4:c.*35-2173G= MANE Select NP_001446.1:n.*35-2173G=
NM_201559.3:c.*35-2173G= NP_963853.1:n.*35-2173G=