Canonical Allele Identifier: CA2086482499
Gene: FOXO1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.40565575T>G , CM000675.2:g.40565575T>G GRCh38
NC_000013.10:g.41139712T>G , CM000675.1:g.41139712T>G GRCh37
NC_000013.9:g.40037712T>G NCBI36
NG_023244.1:g.106023A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000379561.6:c.631-4715A>C MANE Select ENSP00000368880.4:n.631-4715A>C
ENST00000655267.1:n.334-2813A>C
ENST00000660760.1:n.398-4715A>C
ENST00000379561.5:c.631-4715A>C ENSP00000368880.4:n.631-4715A>C
NM_002015.3:c.631-4715A>C NP_002006.2:n.631-4715A>C
XM_011535008.1:c.88-4715A>C XP_011533310.1:n.88-4715A>C
XM_011535009.1:c.76-4715A>C XP_011533311.1:n.76-4715A>C
XR_941536.1:n.1227-4715A>C
XM_011535008.2:c.88-4715A>C XP_011533310.1:n.88-4715A>C
XM_011535010.2:c.-2968A>C XP_011533312.1:n.-2968A>C
NM_002015.4:c.631-4715A>C MANE Select NP_002006.2:n.631-4715A>C