Canonical Allele Identifier: CA2679911222
Gene: FOXO3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.108561626del , CM000668.2:g.108561626del GRCh38
NC_000006.11:g.108882829del , CM000668.1:g.108882829del GRCh37
NC_000006.10:g.108989522del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000406360.2:c.418del MANE Select ENSP00000385824.1:p.Ala140ArgfsTer26
ENST00000343882.10:c.418del ENSP00000339527.6:p.Ala140ArgfsTer26
ENST00000406360.1:c.418del ENSP00000385824.1:p.Ala140ArgfsTer26
NM_001455.3:c.418del NP_001446.1:p.Ala140ArgfsTer26
NM_201559.2:c.418del NP_963853.1:p.Ala140ArgfsTer26
NM_001455.4:c.418del MANE Select NP_001446.1:p.Ala140ArgfsTer26
NM_201559.3:c.418del NP_963853.1:p.Ala140ArgfsTer26