Canonical Allele Identifier: CA1654427934

Gene: FOXO3

Linked Data

• dbSNP Id: rs1254159699

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.108677642C>T , CM000668.2:g.108677642C>T	GRCh38
NC_000006.11:g.108998845C>T , CM000668.1:g.108998845C>T	GRCh37
NC_000006.10:g.109105538C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000406360.2:c.*35-2185C>T MANE Select	ENSP00000385824.1:n.*35-2185C>T
ENST00000343882.10:c.*35-2185C>T	ENSP00000339527.6:n.*35-2185C>T
ENST00000406360.1:c.*35-2185C>T	ENSP00000385824.1:n.*35-2185C>T
ENST00000540898.1:c.*35-2185C>T	ENSP00000446316.1:n.*35-2185C>T
NM_001455.3:c.*35-2185C>T	NP_001446.1:n.*35-2185C>T
NM_201559.2:c.*35-2185C>T	NP_963853.1:n.*35-2185C>T
XM_005266867.3:c.*35-2185C>T	XP_005266924.1:n.*35-2185C>T
XM_005266868.2:c.*35-2185C>T	XP_005266925.1:n.*35-2185C>T
XM_011535626.1:c.*35-2185C>T	XP_011533928.1:n.*35-2185C>T
XM_011535627.1:c.*35-2185C>T	XP_011533929.1:n.*35-2185C>T
XM_011535628.1:c.*35-2185C>T	XP_011533930.1:n.*35-2185C>T
XM_011535629.1:c.*35-2185C>T	XP_011533931.1:n.*35-2185C>T
XM_005266867.4:c.*35-2185C>T	XP_005266924.1:n.*35-2185C>T
XM_005266868.3:c.*35-2185C>T	XP_005266925.1:n.*35-2185C>T
XM_011535626.2:c.*35-2185C>T	XP_011533928.1:n.*35-2185C>T
XM_011535628.3:c.*35-2185C>T	XP_011533930.1:n.*35-2185C>T
XM_011535629.2:c.*35-2185C>T	XP_011533931.1:n.*35-2185C>T
XM_017010585.1:c.*35-2185C>T	XP_016866074.1:n.*35-2185C>T
XM_017010586.1:c.*35-2185C>T	XP_016866075.1:n.*35-2185C>T
NM_001455.4:c.*35-2185C>T MANE Select	NP_001446.1:n.*35-2185C>T
NM_201559.3:c.*35-2185C>T	NP_963853.1:n.*35-2185C>T