Canonical Allele Identifier: CA698022660
Gene: FOXO1 HGNC NCBI

Linked Data

dbSNP Id: rs1246704993

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.40644682_40644683del , CM000675.2:g.40644682_40644683del GRCh38
NC_000013.10:g.41218819_41218820del , CM000675.1:g.41218819_41218820del GRCh37
NC_000013.9:g.40116819_40116820del NCBI36
NG_023244.1:g.26918_26919del

Transcript Alleles

HGVS Amino-acid Change
ENST00000379561.6:c.630+20903_630+20904del MANE Select ENSP00000368880.4:n.630+20903_630+20904del
ENST00000655267.1:n.333+20903_333+20904del
ENST00000660760.1:n.296-11432_296-11431del
ENST00000379561.5:c.630+20903_630+20904del ENSP00000368880.4:n.630+20903_630+20904del
NM_002015.3:c.630+20903_630+20904del NP_002006.2:n.630+20903_630+20904del
XR_941536.1:n.1226+659_1226+660del
NM_002015.4:c.630+20903_630+20904del MANE Select NP_002006.2:n.630+20903_630+20904del