Canonical Allele Identifier: CA2634410384

Gene: WWOX

Linked Data

• gnomAD v4: 16-78108350-ATT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78108352_78108353del , CM000678.2:g.78108352_78108353del	GRCh38
NC_000016.9:g.78142249_78142250del , CM000678.1:g.78142249_78142250del	GRCh37
NC_000016.8:g.76699750_76699751del	NCBI36
NG_011698.1:g.13699_13700del

Transcript Alleles

HGVS	Amino-acid change
ENST00000627394.3:c.108-71_108-70del	ENSP00000485925.2:n.108-71_108-70del
ENST00000682609.1:n.435-71_435-70del
ENST00000683286.1:n.435-71_435-70del
ENST00000683929.1:c.108-71_108-70del	ENSP00000507689.1:n.108-71_108-70del
ENST00000684070.1:n.437-1426_437-1425del
ENST00000684381.1:n.435-71_435-70del
ENST00000684452.1:n.435-71_435-70del
ENST00000684632.1:n.487-71_487-70del
ENST00000566780.6:c.108-71_108-70del MANE Select	ENSP00000457230.1:n.108-71_108-70del
ENST00000355860.7:c.108-71_108-70del	ENSP00000348119.3:n.108-71_108-70del
ENST00000402655.6:c.108-71_108-70del	ENSP00000384238.2:n.108-71_108-70del
ENST00000406884.6:c.108-71_108-70del	ENSP00000384495.2:n.108-71_108-70del
ENST00000408984.7:c.108-71_108-70del	ENSP00000386161.3:n.108-71_108-70del
ENST00000539474.6:c.108-71_108-70del	ENSP00000445210.2:n.108-71_108-70del
ENST00000561846.5:n.152-71_152-70del
ENST00000562214.5:n.231-71_231-70del
ENST00000563358.5:n.215-71_215-70del
ENST00000565562.5:n.153-71_153-70del
ENST00000566662.5:c.108-1426_108-1425del	ENSP00000454331.1:n.108-1426_108-1425del
ENST00000566780.5:c.108-71_108-70del	ENSP00000457230.1:n.108-71_108-70del
ENST00000569332.5:c.108-1426_108-1425del	ENSP00000454788.1:n.108-1426_108-1425del
ENST00000627394.2:c.108-1426_108-1425del	ENSP00000485925.1:n.108-1426_108-1425del
NM_001291997.1:c.-167-1426_-167-1425del	NP_001278926.1:n.-167-1426_-167-1425del
NM_016373.3:c.108-71_108-70del	NP_057457.1:n.108-71_108-70del
NM_130791.3:c.108-71_108-70del	NP_570607.1:n.108-71_108-70del
NR_120436.1:n.588-71_588-70del
XM_006721195.2:c.108-71_108-70del	XP_006721258.1:n.108-71_108-70del
XM_011523100.1:c.108-71_108-70del	XP_011521402.1:n.108-71_108-70del
XM_011523101.1:c.108-71_108-70del	XP_011521403.1:n.108-71_108-70del
XM_011523102.1:c.108-71_108-70del	XP_011521404.1:n.108-71_108-70del
XM_011523103.1:c.108-71_108-70del	XP_011521405.1:n.108-71_108-70del
XM_011523104.1:c.108-71_108-70del	XP_011521406.1:n.108-71_108-70del
XM_011523105.1:c.108-71_108-70del	XP_011521407.1:n.108-71_108-70del
XM_011523101.3:c.108-71_108-70del	XP_011521403.1:n.108-71_108-70del
XM_011523103.3:c.108-71_108-70del	XP_011521405.1:n.108-71_108-70del
XM_011523104.3:c.108-71_108-70del	XP_011521406.1:n.108-71_108-70del
XM_011523105.3:c.108-71_108-70del	XP_011521407.1:n.108-71_108-70del
XM_017023278.2:c.108-71_108-70del	XP_016878767.1:n.108-71_108-70del
NM_016373.4:c.108-71_108-70del MANE Select	NP_057457.1:n.108-71_108-70del
NM_001291997.2:c.-167-1426_-167-1425del	NP_001278926.1:n.-167-1426_-167-1425del
NM_130791.4:c.108-71_108-70del	NP_570607.1:n.108-71_108-70del
NR_120436.2:n.347-71_347-70del
NM_130791.5:c.108-71_108-70del	NP_570607.1:n.108-71_108-70del
NR_120436.3:n.347-71_347-70del