Canonical Allele Identifier: CA13858165
Gene: FOXO1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.40565740G>A , CM000675.2:g.40565740G>A GRCh38
NC_000013.10:g.41139877G>A , CM000675.1:g.41139877G>A GRCh37
NC_000013.9:g.40037877G>A NCBI36
NG_023244.1:g.105858C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000379561.6:c.631-4880C>T MANE Select ENSP00000368880.4:n.631-4880C>T
ENST00000655267.1:n.334-2978C>T
ENST00000660760.1:n.398-4880C>T
ENST00000379561.5:c.631-4880C>T ENSP00000368880.4:n.631-4880C>T
NM_002015.3:c.631-4880C>T NP_002006.2:n.631-4880C>T
XM_011535008.1:c.88-4880C>T XP_011533310.1:n.88-4880C>T
XM_011535009.1:c.76-4880C>T XP_011533311.1:n.76-4880C>T
XR_941536.1:n.1227-4880C>T
XM_011535008.2:c.88-4880C>T XP_011533310.1:n.88-4880C>T
XM_011535010.2:c.-3133C>T XP_011533312.1:n.-3133C>T
NM_002015.4:c.631-4880C>T MANE Select NP_002006.2:n.631-4880C>T
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