Canonical Allele Identifier: CA2086503474
Gene: FOXO1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.40612341C= , CM000675.2:g.40612341C= GRCh38
NC_000013.10:g.41186478C= , CM000675.1:g.41186478C= GRCh37
NC_000013.9:g.40084478C= NCBI36
NG_023244.1:g.59257G=

Transcript Alleles

HGVS Amino-acid change
ENST00000379561.6:c.631-51481G= MANE Select ENSP00000368880.4:n.631-51481G=
ENST00000655267.1:n.334-49579G=
ENST00000660760.1:n.397+20806G=
ENST00000379561.5:c.631-51481G= ENSP00000368880.4:n.631-51481G=
NM_002015.3:c.631-51481G= NP_002006.2:n.631-51481G=
XM_011535008.1:c.87+1809G= XP_011533310.1:n.87+1809G=
XR_941536.1:n.1226+32998G=
XM_011535008.2:c.87+1809G= XP_011533310.1:n.87+1809G=
NM_002015.4:c.631-51481G= MANE Select NP_002006.2:n.631-51481G=
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