Canonical Allele Identifier: CA1654355950
Gene: FOXO3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.108575012A>T , CM000668.2:g.108575012A>T GRCh38
NC_000006.11:g.108896215A>T , CM000668.1:g.108896215A>T GRCh37
NC_000006.10:g.109002908A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000406360.2:c.621+13183A>T MANE Select ENSP00000385824.1:n.621+13183A>T
ENST00000343882.10:c.621+13183A>T ENSP00000339527.6:n.621+13183A>T
ENST00000406360.1:c.621+13183A>T ENSP00000385824.1:n.621+13183A>T
NM_001455.3:c.621+13183A>T NP_001446.1:n.621+13183A>T
NM_201559.2:c.621+13183A>T NP_963853.1:n.621+13183A>T
XM_005266867.3:c.-64+13183A>T XP_005266924.1:n.-64+13183A>T
XM_011535626.1:c.120+12869A>T XP_011533928.1:n.120+12869A>T
XM_005266867.4:c.-64+13183A>T XP_005266924.1:n.-64+13183A>T
XM_011535626.2:c.120+12869A>T XP_011533928.1:n.120+12869A>T
XM_017010585.1:c.-64+5270A>T XP_016866074.1:n.-64+5270A>T
XM_017010586.1:c.-40+5270A>T XP_016866075.1:n.-40+5270A>T
NM_001455.4:c.621+13183A>T MANE Select NP_001446.1:n.621+13183A>T
NM_201559.3:c.621+13183A>T NP_963853.1:n.621+13183A>T