Canonical Allele Identifier: CA2086518006
Gene: FOXO1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.40644676A= , CM000675.2:g.40644676A= GRCh38
NC_000013.10:g.41218813A= , CM000675.1:g.41218813A= GRCh37
NC_000013.9:g.40116813A= NCBI36
NG_023244.1:g.26922T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000379561.6:c.630+20907T= MANE Select ENSP00000368880.4:n.630+20907T=
ENST00000655267.1:n.333+20907T=
ENST00000660760.1:n.296-11428T=
ENST00000379561.5:c.630+20907T= ENSP00000368880.4:n.630+20907T=
NM_002015.3:c.630+20907T= NP_002006.2:n.630+20907T=
XR_941536.1:n.1226+663T=
NM_002015.4:c.630+20907T= MANE Select NP_002006.2:n.630+20907T=
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