Canonical Allele Identifier: CA2086485440
Gene: FOXO1 HGNC NCBI

Linked Data

dbSNP Id: rs2755213

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.40572164T>A , CM000675.2:g.40572164T>A GRCh38
NC_000013.10:g.41146301T>A , CM000675.1:g.41146301T>A GRCh37
NC_000013.9:g.40044301T>A NCBI36
NG_023244.1:g.99434A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000379561.6:c.631-11304A>T MANE Select ENSP00000368880.4:n.631-11304A>T
ENST00000655267.1:n.334-9402A>T
ENST00000660760.1:n.398-11304A>T
ENST00000379561.5:c.631-11304A>T ENSP00000368880.4:n.631-11304A>T
NM_002015.3:c.631-11304A>T NP_002006.2:n.631-11304A>T
XM_011535008.1:c.88-11304A>T XP_011533310.1:n.88-11304A>T
XM_011535009.1:c.76-11304A>T XP_011533311.1:n.76-11304A>T
XR_941536.1:n.1227-11304A>T
XM_011535008.2:c.88-11304A>T XP_011533310.1:n.88-11304A>T
NM_002015.4:c.631-11304A>T MANE Select NP_002006.2:n.631-11304A>T