Canonical Allele Identifier: CA1654427818
Gene: FOXO3 HGNC NCBI

Linked Data

dbSNP Id: rs1770663644

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.108677587_108677588del , CM000668.2:g.108677587_108677588del GRCh38
NC_000006.11:g.108998790_108998791del , CM000668.1:g.108998790_108998791del GRCh37
NC_000006.10:g.109105483_109105484del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000406360.2:c.*35-2240_*35-2239del MANE Select ENSP00000385824.1:n.*35-2240_*35-2239del
ENST00000343882.10:c.*35-2240_*35-2239del ENSP00000339527.6:n.*35-2240_*35-2239del
ENST00000406360.1:c.*35-2240_*35-2239del ENSP00000385824.1:n.*35-2240_*35-2239del
ENST00000540898.1:c.*35-2240_*35-2239del ENSP00000446316.1:n.*35-2240_*35-2239del
NM_001455.3:c.*35-2240_*35-2239del NP_001446.1:n.*35-2240_*35-2239del
NM_201559.2:c.*35-2240_*35-2239del NP_963853.1:n.*35-2240_*35-2239del
XM_005266867.3:c.*35-2240_*35-2239del XP_005266924.1:n.*35-2240_*35-2239del
XM_005266868.2:c.*35-2240_*35-2239del XP_005266925.1:n.*35-2240_*35-2239del
XM_011535626.1:c.*35-2240_*35-2239del XP_011533928.1:n.*35-2240_*35-2239del
XM_011535627.1:c.*35-2240_*35-2239del XP_011533929.1:n.*35-2240_*35-2239del
XM_011535628.1:c.*35-2240_*35-2239del XP_011533930.1:n.*35-2240_*35-2239del
XM_011535629.1:c.*35-2240_*35-2239del XP_011533931.1:n.*35-2240_*35-2239del
XM_005266867.4:c.*35-2240_*35-2239del XP_005266924.1:n.*35-2240_*35-2239del
XM_005266868.3:c.*35-2240_*35-2239del XP_005266925.1:n.*35-2240_*35-2239del
XM_011535626.2:c.*35-2240_*35-2239del XP_011533928.1:n.*35-2240_*35-2239del
XM_011535628.3:c.*35-2240_*35-2239del XP_011533930.1:n.*35-2240_*35-2239del
XM_011535629.2:c.*35-2240_*35-2239del XP_011533931.1:n.*35-2240_*35-2239del
XM_017010585.1:c.*35-2240_*35-2239del XP_016866074.1:n.*35-2240_*35-2239del
XM_017010586.1:c.*35-2240_*35-2239del XP_016866075.1:n.*35-2240_*35-2239del
NM_001455.4:c.*35-2240_*35-2239del MANE Select NP_001446.1:n.*35-2240_*35-2239del
NM_201559.3:c.*35-2240_*35-2239del NP_963853.1:n.*35-2240_*35-2239del