Canonical Allele Identifier: CA2086517795
Gene: FOXO1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.40644239_40644240delinsCA , CM000675.2:g.40644239_40644240delinsCA GRCh38
NC_000013.10:g.41218376_41218377delinsCA , CM000675.1:g.41218376_41218377delinsCA GRCh37
NC_000013.9:g.40116376_40116377delinsCA NCBI36
NG_023244.1:g.27358_27359delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000379561.6:c.630+21343_630+21344delinsTG MANE Select ENSP00000368880.4:n.630+21343_630+21344delinsTG
ENST00000655267.1:n.333+21343_333+21344delinsTG
ENST00000660760.1:n.296-10992_296-10991delinsTG
ENST00000379561.5:c.630+21343_630+21344delinsTG ENSP00000368880.4:n.630+21343_630+21344delinsTG
NM_002015.3:c.630+21343_630+21344delinsTG NP_002006.2:n.630+21343_630+21344delinsTG
XR_941536.1:n.1226+1099_1226+1100delinsTG
NM_002015.4:c.630+21343_630+21344delinsTG MANE Select NP_002006.2:n.630+21343_630+21344delinsTG