Canonical Allele Identifier: CA2086517782
Gene: FOXO1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.40644215G= , CM000675.2:g.40644215G= GRCh38
NC_000013.10:g.41218352G= , CM000675.1:g.41218352G= GRCh37
NC_000013.9:g.40116352G= NCBI36
NG_023244.1:g.27383C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000379561.6:c.630+21368C= MANE Select ENSP00000368880.4:n.630+21368C=
ENST00000655267.1:n.333+21368C=
ENST00000660760.1:n.296-10967C=
ENST00000379561.5:c.630+21368C= ENSP00000368880.4:n.630+21368C=
NM_002015.3:c.630+21368C= NP_002006.2:n.630+21368C=
XR_941536.1:n.1226+1124C=
NM_002015.4:c.630+21368C= MANE Select NP_002006.2:n.630+21368C=
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