Canonical Allele Identifier: CA145715567

Gene: FOXO3

Linked Data

• dbSNP Id: rs10583126
• gnomAD v2: 6-108913089-TAA-T
• gnomAD v3: 6-108591886-TAA-T
• gnomAD v4: 6-108591886-TAA-T
• MyVariant Identifiers: chr6:g.108913091_108913092del (hg19) ; chr6:g.108913090_108913091del (hg19) ; chr6:g.108591888_108591889del (hg38) ; chr6:g.108591887_108591888del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.108591899_108591900del , CM000668.2:g.108591899_108591900del	GRCh38
NC_000006.11:g.108913102_108913103del , CM000668.1:g.108913102_108913103del	GRCh37
NC_000006.10:g.109019795_109019796del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000406360.2:c.621+30070_621+30071del MANE Select	ENSP00000385824.1:n.621+30070_621+30071del
ENST00000343882.10:c.621+30070_621+30071del	ENSP00000339527.6:n.621+30070_621+30071del
ENST00000406360.1:c.621+30070_621+30071del	ENSP00000385824.1:n.621+30070_621+30071del
NM_001455.3:c.621+30070_621+30071del	NP_001446.1:n.621+30070_621+30071del
NM_201559.2:c.621+30070_621+30071del	NP_963853.1:n.621+30070_621+30071del
XM_005266867.3:c.-64+30070_-64+30071del	XP_005266924.1:n.-64+30070_-64+30071del
XM_011535626.1:c.120+29756_120+29757del	XP_011533928.1:n.120+29756_120+29757del
XM_011535627.1:c.69+5263_69+5264del	XP_011533929.1:n.69+5263_69+5264del
XM_011535628.1:c.-40+2084_-40+2085del	XP_011533930.1:n.-40+2084_-40+2085del
XM_005266867.4:c.-64+30070_-64+30071del	XP_005266924.1:n.-64+30070_-64+30071del
XM_011535626.2:c.120+29756_120+29757del	XP_011533928.1:n.120+29756_120+29757del
XM_011535628.3:c.-40+2084_-40+2085del	XP_011533930.1:n.-40+2084_-40+2085del
XM_017010585.1:c.-64+22157_-64+22158del	XP_016866074.1:n.-64+22157_-64+22158del
XM_017010586.1:c.-40+22157_-40+22158del	XP_016866075.1:n.-40+22157_-40+22158del
NM_001455.4:c.621+30070_621+30071del MANE Select	NP_001446.1:n.621+30070_621+30071del
NM_201559.3:c.621+30070_621+30071del	NP_963853.1:n.621+30070_621+30071del