Canonical Allele Identifier: CA2086517832
Gene: FOXO1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.40644310_40644313delinsACTC , CM000675.2:g.40644310_40644313delinsACTC GRCh38
NC_000013.10:g.41218447_41218450delinsACTC , CM000675.1:g.41218447_41218450delinsACTC GRCh37
NC_000013.9:g.40116447_40116450delinsACTC NCBI36
NG_023244.1:g.27285_27288delinsGAGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000379561.6:c.630+21270_630+21273delinsGAGT MANE Select ENSP00000368880.4:n.630+21270_630+21273delinsGAGT
ENST00000655267.1:n.333+21270_333+21273delinsGAGT
ENST00000660760.1:n.296-11065_296-11062delinsGAGT
ENST00000379561.5:c.630+21270_630+21273delinsGAGT ENSP00000368880.4:n.630+21270_630+21273delinsGAGT
NM_002015.3:c.630+21270_630+21273delinsGAGT NP_002006.2:n.630+21270_630+21273delinsGAGT
XR_941536.1:n.1226+1026_1226+1029delinsGAGT
NM_002015.4:c.630+21270_630+21273delinsGAGT MANE Select NP_002006.2:n.630+21270_630+21273delinsGAGT