Canonical Allele Identifier: CA1654331924

Gene: FOXO3

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.108613251_108613253delinsCTT , CM000668.2:g.108613251_108613253delinsCTT	GRCh38
NC_000006.11:g.108934454_108934456delinsCTT , CM000668.1:g.108934454_108934456delinsCTT	GRCh37
NC_000006.10:g.109041147_109041149delinsCTT	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000406360.2:c.622-50204_622-50202delinsCTT MANE Select	ENSP00000385824.1:n.622-50204_622-50202delinsCTT
ENST00000343882.10:c.622-50204_622-50202delinsCTT	ENSP00000339527.6:n.622-50204_622-50202delinsCTT
ENST00000406360.1:c.622-50204_622-50202delinsCTT	ENSP00000385824.1:n.622-50204_622-50202delinsCTT
NM_001455.3:c.622-50204_622-50202delinsCTT	NP_001446.1:n.622-50204_622-50202delinsCTT
NM_201559.2:c.622-50204_622-50202delinsCTT	NP_963853.1:n.622-50204_622-50202delinsCTT
XM_005266867.3:c.-63-26242_-63-26240delinsCTT	XP_005266924.1:n.-63-26242_-63-26240delinsCTT
XM_011535626.1:c.121-50204_121-50202delinsCTT	XP_011533928.1:n.121-50204_121-50202delinsCTT
XM_011535627.1:c.69+26615_69+26617delinsCTT	XP_011533929.1:n.69+26615_69+26617delinsCTT
XM_011535628.1:c.-40+23436_-40+23438delinsCTT	XP_011533930.1:n.-40+23436_-40+23438delinsCTT
XM_005266867.4:c.-63-26242_-63-26240delinsCTT	XP_005266924.1:n.-63-26242_-63-26240delinsCTT
XM_011535626.2:c.121-50204_121-50202delinsCTT	XP_011533928.1:n.121-50204_121-50202delinsCTT
XM_011535628.3:c.-40+23436_-40+23438delinsCTT	XP_011533930.1:n.-40+23436_-40+23438delinsCTT
XM_017010585.1:c.-63-26242_-63-26240delinsCTT	XP_016866074.1:n.-63-26242_-63-26240delinsCTT
XM_017010586.1:c.-40+43509_-40+43511delinsCTT	XP_016866075.1:n.-40+43509_-40+43511delinsCTT
NM_001455.4:c.622-50204_622-50202delinsCTT MANE Select	NP_001446.1:n.622-50204_622-50202delinsCTT
NM_201559.3:c.622-50204_622-50202delinsCTT	NP_963853.1:n.622-50204_622-50202delinsCTT