Canonical Allele Identifier: CA1654331903
Gene: FOXO3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.108613189A= , CM000668.2:g.108613189A= GRCh38
NC_000006.11:g.108934392A= , CM000668.1:g.108934392A= GRCh37
NC_000006.10:g.109041085A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000406360.2:c.622-50266A= MANE Select ENSP00000385824.1:n.622-50266A=
ENST00000343882.10:c.622-50266A= ENSP00000339527.6:n.622-50266A=
ENST00000406360.1:c.622-50266A= ENSP00000385824.1:n.622-50266A=
NM_001455.3:c.622-50266A= NP_001446.1:n.622-50266A=
NM_201559.2:c.622-50266A= NP_963853.1:n.622-50266A=
XM_005266867.3:c.-63-26304A= XP_005266924.1:n.-63-26304A=
XM_011535626.1:c.121-50266A= XP_011533928.1:n.121-50266A=
XM_011535627.1:c.69+26553A= XP_011533929.1:n.69+26553A=
XM_011535628.1:c.-40+23374A= XP_011533930.1:n.-40+23374A=
XM_005266867.4:c.-63-26304A= XP_005266924.1:n.-63-26304A=
XM_011535626.2:c.121-50266A= XP_011533928.1:n.121-50266A=
XM_011535628.3:c.-40+23374A= XP_011533930.1:n.-40+23374A=
XM_017010585.1:c.-63-26304A= XP_016866074.1:n.-63-26304A=
XM_017010586.1:c.-40+43447A= XP_016866075.1:n.-40+43447A=
NM_001455.4:c.622-50266A= MANE Select NP_001446.1:n.622-50266A=
NM_201559.3:c.622-50266A= NP_963853.1:n.622-50266A=