Canonical Allele Identifier: CA2086517769
Gene: FOXO1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.40644177G= , CM000675.2:g.40644177G= GRCh38
NC_000013.10:g.41218314G= , CM000675.1:g.41218314G= GRCh37
NC_000013.9:g.40116314G= NCBI36
NG_023244.1:g.27421C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000379561.6:c.630+21406C= MANE Select ENSP00000368880.4:n.630+21406C=
ENST00000655267.1:n.333+21406C=
ENST00000660760.1:n.296-10929C=
ENST00000379561.5:c.630+21406C= ENSP00000368880.4:n.630+21406C=
NM_002015.3:c.630+21406C= NP_002006.2:n.630+21406C=
XR_941536.1:n.1226+1162C=
NM_002015.4:c.630+21406C= MANE Select NP_002006.2:n.630+21406C=
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