Canonical Allele Identifier: CA284502104

Gene: WWOX

Linked Data

• dbSNP Id: rs890715320
• gnomAD v3: 16-78099685-ACG-A
• gnomAD v4: 16-78099685-ACG-A
• MyVariant Identifiers: chr16:g.78133583_78133584del (hg19) ; chr16:g.78099686_78099687del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78099692_78099693del , CM000678.2:g.78099692_78099693del	GRCh38
NC_000016.9:g.78133589_78133590del , CM000678.1:g.78133589_78133590del	GRCh37
NC_000016.8:g.76691090_76691091del	NCBI36
NG_011698.1:g.5039_5040del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627394.3:c.-87_-86del	ENSP00000485925.2:n.-87_-86del
ENST00000682609.1:n.241_242del
ENST00000683286.1:n.241_242del
ENST00000683929.1:c.-87_-86del	ENSP00000507689.1:n.-87_-86del
ENST00000684070.1:n.243_244del
ENST00000684381.1:n.241_242del
ENST00000684452.1:n.241_242del
ENST00000684632.1:n.293_294del
ENST00000566780.6:c.-87_-86del MANE Select	ENSP00000457230.1:n.-87_-86del
ENST00000355860.7:c.-87_-86del	ENSP00000348119.3:n.-87_-86del
ENST00000402655.6:c.-87_-86del	ENSP00000384238.2:n.-87_-86del
ENST00000406884.6:c.-87_-86del	ENSP00000384495.2:n.-87_-86del
ENST00000539474.6:c.-87_-86del	ENSP00000445210.2:n.-87_-86del
ENST00000562214.5:n.37_38del
ENST00000566662.5:c.-87_-86del	ENSP00000454331.1:n.-87_-86del
ENST00000566780.5:c.-87_-86del	ENSP00000457230.1:n.-87_-86del
ENST00000569332.5:c.-87_-86del	ENSP00000454788.1:n.-87_-86del
ENST00000569818.1:c.-87_-86del	ENSP00000454485.1:n.-87_-86del
ENST00000627394.2:c.-87_-86del	ENSP00000485925.1:n.-87_-86del
NM_001291997.1:c.-361_-360del	NP_001278926.1:n.-361_-360del
NM_016373.3:c.-87_-86del	NP_057457.1:n.-87_-86del
NM_130791.3:c.-87_-86del	NP_570607.1:n.-87_-86del
NR_120435.1:n.280_281del
NR_120436.1:n.280_281del
XM_006721195.2:c.-87_-86del	XP_006721258.1:n.-87_-86del
XM_011523100.1:c.-87_-86del	XP_011521402.1:n.-87_-86del
XM_011523101.1:c.-87_-86del	XP_011521403.1:n.-87_-86del
XM_011523102.1:c.-87_-86del	XP_011521404.1:n.-87_-86del
XM_011523103.1:c.-87_-86del	XP_011521405.1:n.-87_-86del
XM_011523104.1:c.-87_-86del	XP_011521406.1:n.-87_-86del
XM_011523105.1:c.-87_-86del	XP_011521407.1:n.-87_-86del
XM_011523101.3:c.-87_-86del	XP_011521403.1:n.-87_-86del
XM_011523103.3:c.-87_-86del	XP_011521405.1:n.-87_-86del
XM_011523104.3:c.-87_-86del	XP_011521406.1:n.-87_-86del
XM_011523105.3:c.-87_-86del	XP_011521407.1:n.-87_-86del
XM_017023278.2:c.-87_-86del	XP_016878767.1:n.-87_-86del
NM_016373.4:c.-87_-86del MANE Select	NP_057457.1:n.-87_-86del
NM_001291997.2:c.-361_-360del	NP_001278926.1:n.-361_-360del
NM_130791.4:c.-87_-86del	NP_570607.1:n.-87_-86del
NR_120435.2:n.39_40del
NR_120436.2:n.39_40del
NM_130791.5:c.-87_-86del	NP_570607.1:n.-87_-86del
NR_120436.3:n.39_40del