Canonical Allele Identifier: CA1092992428
Gene: FOXO3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.108591902_108591905del , CM000668.2:g.108591902_108591905del GRCh38
NC_000006.11:g.108913105_108913108del , CM000668.1:g.108913105_108913108del GRCh37
NC_000006.10:g.109019798_109019801del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000406360.2:c.621+30073_621+30076del MANE Select ENSP00000385824.1:n.621+30073_621+30076del
ENST00000343882.10:c.621+30073_621+30076del ENSP00000339527.6:n.621+30073_621+30076del
ENST00000406360.1:c.621+30073_621+30076del ENSP00000385824.1:n.621+30073_621+30076del
NM_001455.3:c.621+30073_621+30076del NP_001446.1:n.621+30073_621+30076del
NM_201559.2:c.621+30073_621+30076del NP_963853.1:n.621+30073_621+30076del
XM_005266867.3:c.-64+30073_-64+30076del XP_005266924.1:n.-64+30073_-64+30076del
XM_011535626.1:c.120+29759_120+29762del XP_011533928.1:n.120+29759_120+29762del
XM_011535627.1:c.69+5266_69+5269del XP_011533929.1:n.69+5266_69+5269del
XM_011535628.1:c.-40+2087_-40+2090del XP_011533930.1:n.-40+2087_-40+2090del
XM_005266867.4:c.-64+30073_-64+30076del XP_005266924.1:n.-64+30073_-64+30076del
XM_011535626.2:c.120+29759_120+29762del XP_011533928.1:n.120+29759_120+29762del
XM_011535628.3:c.-40+2087_-40+2090del XP_011533930.1:n.-40+2087_-40+2090del
XM_017010585.1:c.-64+22160_-64+22163del XP_016866074.1:n.-64+22160_-64+22163del
XM_017010586.1:c.-40+22160_-40+22163del XP_016866075.1:n.-40+22160_-40+22163del
NM_001455.4:c.621+30073_621+30076del MANE Select NP_001446.1:n.621+30073_621+30076del
NM_201559.3:c.621+30073_621+30076del NP_963853.1:n.621+30073_621+30076del