Canonical Allele Identifier: CA979375536

Gene: WWOX

Linked Data

• dbSNP Id: rs2083242064
• gnomAD v3: 16-78432374-CG-C
• gnomAD v4: 16-78432374-CG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78432376del , CM000678.2:g.78432376del	GRCh38
NC_000016.9:g.78466273del , CM000678.1:g.78466273del	GRCh37
NC_000016.8:g.77023774del	NCBI36
NG_011698.1:g.337723del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627394.3:c.792-112del	ENSP00000485925.2:n.792-112del
ENST00000683929.1:c.792-112del	ENSP00000507689.1:n.792-112del
ENST00000684632.1:n.1171-112del
ENST00000566780.6:c.792-112del MANE Select	ENSP00000457230.1:n.792-112del
ENST00000402655.6:c.409+317222del	ENSP00000384238.2:n.409+317222del
ENST00000406884.6:c.516+268087del	ENSP00000384495.2:n.516+268087del
ENST00000408984.7:c.792-112del	ENSP00000386161.3:n.792-112del
ENST00000539474.6:c.409+317222del	ENSP00000445210.2:n.409+317222del
ENST00000562639.5:n.480-112del
ENST00000566780.5:c.792-112del	ENSP00000457230.1:n.792-112del
ENST00000569332.5:c.*589-112del	ENSP00000454788.1:n.*589-112del
ENST00000620008.1:c.186-112del	ENSP00000482648.1:n.186-112del
NM_001291997.1:c.453-112del	NP_001278926.1:n.453-112del
NM_016373.3:c.792-112del	NP_057457.1:n.792-112del
XM_006721195.2:c.792-112del	XP_006721258.1:n.792-112del
XM_011523100.1:c.792-112del	XP_011521402.1:n.792-112del
XM_011523101.1:c.792-112del	XP_011521403.1:n.792-112del
XM_011523102.1:c.792-112del	XP_011521404.1:n.792-112del
XM_011523103.1:c.792-112del	XP_011521405.1:n.792-112del
XM_011523104.1:c.792-112del	XP_011521406.1:n.792-112del
XR_933765.1:n.3419-1562del
XM_011523101.3:c.792-112del	XP_011521403.1:n.792-112del
XM_011523103.3:c.792-112del	XP_011521405.1:n.792-112del
XM_011523104.3:c.792-112del	XP_011521406.1:n.792-112del
NM_016373.4:c.792-112del MANE Select	NP_057457.1:n.792-112del
NM_001291997.2:c.453-112del	NP_001278926.1:n.453-112del