Canonical Allele Identifier: CA724219022

Gene: WWOX

Linked Data

• dbSNP Id: rs1213748660
• gnomAD v3: 16-78154739-ATAG-A
• gnomAD v4: 16-78154739-ATAG-A
• MyVariant Identifiers: chr16:g.78188637_78188639del (hg19) ; chr16:g.78154740_78154742del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78154741_78154743del , CM000678.2:g.78154741_78154743del	GRCh38
NC_000016.9:g.78188638_78188640del , CM000678.1:g.78188638_78188640del	GRCh37
NC_000016.8:g.76746139_76746141del	NCBI36
NG_011698.1:g.60088_60090del

Transcript Alleles

HGVS	Amino-acid change
ENST00000627394.3:c.410-9442_410-9440del	ENSP00000485925.2:n.410-9442_410-9440del
ENST00000683286.1:n.737-9442_737-9440del
ENST00000683929.1:c.410-9442_410-9440del	ENSP00000507689.1:n.410-9442_410-9440del
ENST00000684070.1:n.674-9442_674-9440del
ENST00000684632.1:n.789-9442_789-9440del
ENST00000566780.6:c.410-9442_410-9440del MANE Select	ENSP00000457230.1:n.410-9442_410-9440del
ENST00000355860.7:c.410-9442_410-9440del	ENSP00000348119.3:n.410-9442_410-9440del
ENST00000402655.6:c.409+39587_409+39589del	ENSP00000384238.2:n.409+39587_409+39589del
ENST00000406884.6:c.410-9442_410-9440del	ENSP00000384495.2:n.410-9442_410-9440del
ENST00000408984.7:c.410-9442_410-9440del	ENSP00000386161.3:n.410-9442_410-9440del
ENST00000539474.6:c.409+39587_409+39589del	ENSP00000445210.2:n.409+39587_409+39589del
ENST00000561846.5:n.454-9442_454-9440del
ENST00000562639.5:n.98-9442_98-9440del
ENST00000563358.5:n.517-9442_517-9440del
ENST00000565791.1:n.17+8808_17+8810del
ENST00000566662.5:c.*28-9442_*28-9440del	ENSP00000454331.1:n.*28-9442_*28-9440del
ENST00000566780.5:c.410-9442_410-9440del	ENSP00000457230.1:n.410-9442_410-9440del
ENST00000569332.5:c.*207-9442_*207-9440del	ENSP00000454788.1:n.*207-9442_*207-9440del
ENST00000627394.2:c.*207-9442_*207-9440del	ENSP00000485925.1:n.*207-9442_*207-9440del
NM_001291997.1:c.71-9442_71-9440del	NP_001278926.1:n.71-9442_71-9440del
NM_016373.3:c.410-9442_410-9440del	NP_057457.1:n.410-9442_410-9440del
NM_130791.3:c.410-9442_410-9440del	NP_570607.1:n.410-9442_410-9440del
NR_120436.1:n.890-9442_890-9440del
XM_006721195.2:c.410-9442_410-9440del	XP_006721258.1:n.410-9442_410-9440del
XM_011523100.1:c.410-9442_410-9440del	XP_011521402.1:n.410-9442_410-9440del
XM_011523101.1:c.410-9442_410-9440del	XP_011521403.1:n.410-9442_410-9440del
XM_011523102.1:c.410-9442_410-9440del	XP_011521404.1:n.410-9442_410-9440del
XM_011523103.1:c.410-9442_410-9440del	XP_011521405.1:n.410-9442_410-9440del
XM_011523104.1:c.410-9442_410-9440del	XP_011521406.1:n.410-9442_410-9440del
XM_011523105.1:c.410-9442_410-9440del	XP_011521407.1:n.410-9442_410-9440del
XM_011523101.3:c.410-9442_410-9440del	XP_011521403.1:n.410-9442_410-9440del
XM_011523103.3:c.410-9442_410-9440del	XP_011521405.1:n.410-9442_410-9440del
XM_011523104.3:c.410-9442_410-9440del	XP_011521406.1:n.410-9442_410-9440del
XM_011523105.3:c.410-9442_410-9440del	XP_011521407.1:n.410-9442_410-9440del
XM_017023278.2:c.410-9442_410-9440del	XP_016878767.1:n.410-9442_410-9440del
NM_016373.4:c.410-9442_410-9440del MANE Select	NP_057457.1:n.410-9442_410-9440del
NM_001291997.2:c.71-9442_71-9440del	NP_001278926.1:n.71-9442_71-9440del
NM_130791.4:c.410-9442_410-9440del	NP_570607.1:n.410-9442_410-9440del
NR_120436.2:n.649-9442_649-9440del
NM_130791.5:c.410-9442_410-9440del	NP_570607.1:n.410-9442_410-9440del
NR_120436.3:n.649-9442_649-9440del