Canonical Allele Identifier: CA698022391
Gene: FOXO1 HGNC NCBI

Linked Data

dbSNP Id: rs1370683928
MyVariant Identifiers: chr13:g.41218333_41218334insA (hg19) chr13:g.40644196_40644197insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.40644197dup , CM000675.2:g.40644197dup GRCh38
NC_000013.10:g.41218334dup , CM000675.1:g.41218334dup GRCh37
NC_000013.9:g.40116334dup NCBI36
NG_023244.1:g.27401dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000379561.6:c.630+21386dup MANE Select ENSP00000368880.4:n.630+21386dup
ENST00000655267.1:n.333+21386dup
ENST00000660760.1:n.296-10949dup
ENST00000379561.5:c.630+21386dup ENSP00000368880.4:n.630+21386dup
NM_002015.3:c.630+21386dup NP_002006.2:n.630+21386dup
XR_941536.1:n.1226+1142dup
NM_002015.4:c.630+21386dup MANE Select NP_002006.2:n.630+21386dup
Search 100 bp 5'
Search 100 bp 3'