Canonical Allele Identifier: CA2234901756

Gene: WWOX

Linked Data

• ClinVar Variation Id: 1938931
• ClinVar RCV Id: RCV002666550
• dbSNP Id: rs2032287989

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78108423_78108427dup , CM000678.2:g.78108423_78108427dup	GRCh38
NC_000016.9:g.78142320_78142324dup , CM000678.1:g.78142320_78142324dup	GRCh37
NC_000016.8:g.76699821_76699825dup	NCBI36
NG_011698.1:g.13770_13774dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627394.3:c.108_112dup	ENSP00000485925.2:p.Thr38IlefsTer?
ENST00000682609.1:n.435_439dup
ENST00000683286.1:n.435_439dup
ENST00000683929.1:c.108_112dup	ENSP00000507689.1:p.Thr38IlefsTer?
ENST00000684070.1:n.437-1355_437-1351dup
ENST00000684381.1:n.435_439dup
ENST00000684452.1:n.435_439dup
ENST00000684632.1:n.487_491dup
ENST00000566780.6:c.108_112dup MANE Select	ENSP00000457230.1:p.Thr38IlefsTer?
ENST00000355860.7:c.108_112dup	ENSP00000348119.3:p.Thr38IlefsTer?
ENST00000402655.6:c.108_112dup	ENSP00000384238.2:p.Thr38IlefsTer?
ENST00000406884.6:c.108_112dup	ENSP00000384495.2:p.Thr38IlefsTer?
ENST00000408984.7:c.108_112dup	ENSP00000386161.3:p.Thr38IlefsTer?
ENST00000539474.6:c.108_112dup	ENSP00000445210.2:p.Thr38IlefsTer?
ENST00000561846.5:n.152_156dup
ENST00000562214.5:n.231_235dup
ENST00000563358.5:n.215_219dup
ENST00000565562.5:n.153_157dup
ENST00000566662.5:c.108-1355_108-1351dup	ENSP00000454331.1:n.108-1355_108-1351dup
ENST00000566780.5:c.108_112dup	ENSP00000457230.1:p.Thr38IlefsTer?
ENST00000569332.5:c.108-1355_108-1351dup	ENSP00000454788.1:n.108-1355_108-1351dup
ENST00000627394.2:c.108-1355_108-1351dup	ENSP00000485925.1:n.108-1355_108-1351dup
NM_001291997.1:c.-167-1355_-167-1351dup	NP_001278926.1:n.-167-1355_-167-1351dup
NM_016373.3:c.108_112dup	NP_057457.1:p.Thr38IlefsTer?
NM_130791.3:c.108_112dup	NP_570607.1:p.Thr38IlefsTer?
NR_120436.1:n.588_592dup
XM_006721195.2:c.108_112dup	XP_006721258.1:p.Thr38IlefsTer?
XM_011523100.1:c.108_112dup	XP_011521402.1:p.Thr38IlefsTer?
XM_011523101.1:c.108_112dup	XP_011521403.1:p.Thr38IlefsTer?
XM_011523102.1:c.108_112dup	XP_011521404.1:p.Thr38IlefsTer?
XM_011523103.1:c.108_112dup	XP_011521405.1:p.Thr38IlefsTer?
XM_011523104.1:c.108_112dup	XP_011521406.1:p.Thr38IlefsTer?
XM_011523105.1:c.108_112dup	XP_011521407.1:p.Thr38IlefsTer?
XM_011523101.3:c.108_112dup	XP_011521403.1:p.Thr38IlefsTer?
XM_011523103.3:c.108_112dup	XP_011521405.1:p.Thr38IlefsTer?
XM_011523104.3:c.108_112dup	XP_011521406.1:p.Thr38IlefsTer?
XM_011523105.3:c.108_112dup	XP_011521407.1:p.Thr38IlefsTer?
XM_017023278.2:c.108_112dup	XP_016878767.1:p.Thr38IlefsTer?
NM_016373.4:c.108_112dup MANE Select	NP_057457.1:p.Thr38IlefsTer?
NM_001291997.2:c.-167-1355_-167-1351dup	NP_001278926.1:n.-167-1355_-167-1351dup
NM_130791.4:c.108_112dup	NP_570607.1:p.Thr38IlefsTer?
NR_120436.2:n.347_351dup
NM_130791.5:c.108_112dup	NP_570607.1:p.Thr38IlefsTer?
NR_120436.3:n.347_351dup