Canonical Allele Identifier: CA2086517798
Gene: FOXO1 HGNC NCBI

Linked Data

dbSNP Id: rs1877443177

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.40644243dup , CM000675.2:g.40644243dup GRCh38
NC_000013.10:g.41218380dup , CM000675.1:g.41218380dup GRCh37
NC_000013.9:g.40116380dup NCBI36
NG_023244.1:g.27355dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000379561.6:c.630+21340dup MANE Select ENSP00000368880.4:n.630+21340dup
ENST00000655267.1:n.333+21340dup
ENST00000660760.1:n.296-10995dup
ENST00000379561.5:c.630+21340dup ENSP00000368880.4:n.630+21340dup
NM_002015.3:c.630+21340dup NP_002006.2:n.630+21340dup
XR_941536.1:n.1226+1096dup
NM_002015.4:c.630+21340dup MANE Select NP_002006.2:n.630+21340dup