Canonical Allele Identifier: CA145717804

Gene: FOXO3

Linked Data

• dbSNP Id: rs769085958
• gnomAD v2: 6-108934454-CTT-C
• gnomAD v3: 6-108613251-CTT-C
• gnomAD v4: 6-108613251-CTT-C
• MyVariant Identifiers: chr6:g.108934455_108934456del (hg19) ; chr6:g.108613252_108613253del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.108613252_108613253del , CM000668.2:g.108613252_108613253del	GRCh38
NC_000006.11:g.108934455_108934456del , CM000668.1:g.108934455_108934456del	GRCh37
NC_000006.10:g.109041148_109041149del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406360.2:c.622-50203_622-50202del MANE Select	ENSP00000385824.1:n.622-50203_622-50202del
ENST00000343882.10:c.622-50203_622-50202del	ENSP00000339527.6:n.622-50203_622-50202del
ENST00000406360.1:c.622-50203_622-50202del	ENSP00000385824.1:n.622-50203_622-50202del
NM_001455.3:c.622-50203_622-50202del	NP_001446.1:n.622-50203_622-50202del
NM_201559.2:c.622-50203_622-50202del	NP_963853.1:n.622-50203_622-50202del
XM_005266867.3:c.-63-26241_-63-26240del	XP_005266924.1:n.-63-26241_-63-26240del
XM_011535626.1:c.121-50203_121-50202del	XP_011533928.1:n.121-50203_121-50202del
XM_011535627.1:c.69+26616_69+26617del	XP_011533929.1:n.69+26616_69+26617del
XM_011535628.1:c.-40+23437_-40+23438del	XP_011533930.1:n.-40+23437_-40+23438del
XM_005266867.4:c.-63-26241_-63-26240del	XP_005266924.1:n.-63-26241_-63-26240del
XM_011535626.2:c.121-50203_121-50202del	XP_011533928.1:n.121-50203_121-50202del
XM_011535628.3:c.-40+23437_-40+23438del	XP_011533930.1:n.-40+23437_-40+23438del
XM_017010585.1:c.-63-26241_-63-26240del	XP_016866074.1:n.-63-26241_-63-26240del
XM_017010586.1:c.-40+43510_-40+43511del	XP_016866075.1:n.-40+43510_-40+43511del
NM_001455.4:c.622-50203_622-50202del MANE Select	NP_001446.1:n.622-50203_622-50202del
NM_201559.3:c.622-50203_622-50202del	NP_963853.1:n.622-50203_622-50202del