Canonical Allele Identifier: CA2634410025

Gene: WWOX

Linked Data

• gnomAD v4: 16-78099789-TGCGCTAC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78099793_78099799del , CM000678.2:g.78099793_78099799del	GRCh38
NC_000016.9:g.78133690_78133696del , CM000678.1:g.78133690_78133696del	GRCh37
NC_000016.8:g.76691191_76691197del	NCBI36
NG_011698.1:g.5140_5146del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627394.3:c.15_21del	ENSP00000485925.2:p.Tyr6GlyfsTer?
ENST00000682609.1:n.342_348del
ENST00000683286.1:n.342_348del
ENST00000683929.1:c.15_21del	ENSP00000507689.1:p.Tyr6GlyfsTer?
ENST00000684070.1:n.344_350del
ENST00000684381.1:n.342_348del
ENST00000684452.1:n.342_348del
ENST00000684632.1:n.394_400del
ENST00000566780.6:c.15_21del MANE Select	ENSP00000457230.1:p.Tyr6GlyfsTer?
ENST00000355860.7:c.15_21del	ENSP00000348119.3:p.Tyr6GlyfsTer?
ENST00000402655.6:c.15_21del	ENSP00000384238.2:p.Tyr6GlyfsTer?
ENST00000406884.6:c.15_21del	ENSP00000384495.2:p.Tyr6GlyfsTer?
ENST00000408984.7:c.15_21del	ENSP00000386161.3:p.Tyr6GlyfsTer?
ENST00000539474.6:c.15_21del	ENSP00000445210.2:p.Tyr6GlyfsTer?
ENST00000561846.5:n.59_65del
ENST00000562214.5:n.138_144del
ENST00000563358.5:n.8_14del
ENST00000565562.5:n.60_66del
ENST00000566662.5:c.15_21del	ENSP00000454331.1:p.Tyr6GlyfsTer?
ENST00000566780.5:c.15_21del	ENSP00000457230.1:p.Tyr6GlyfsTer?
ENST00000569332.5:c.15_21del	ENSP00000454788.1:p.Tyr6GlyfsTer?
ENST00000569818.1:c.15_21del	ENSP00000454485.1:p.Tyr6GlyfsTer?
ENST00000627394.2:c.15_21del	ENSP00000485925.1:p.Tyr6GlyfsTer?
NM_001291997.1:c.-260_-254del	NP_001278926.1:n.-260_-254del
NM_016373.3:c.15_21del	NP_057457.1:p.Tyr6GlyfsTer?
NM_130791.3:c.15_21del	NP_570607.1:p.Tyr6GlyfsTer?
NR_120435.1:n.381_387del
NR_120436.1:n.381_387del
XM_006721195.2:c.15_21del	XP_006721258.1:p.Tyr6GlyfsTer?
XM_011523100.1:c.15_21del	XP_011521402.1:p.Tyr6GlyfsTer?
XM_011523101.1:c.15_21del	XP_011521403.1:p.Tyr6GlyfsTer?
XM_011523102.1:c.15_21del	XP_011521404.1:p.Tyr6GlyfsTer?
XM_011523103.1:c.15_21del	XP_011521405.1:p.Tyr6GlyfsTer?
XM_011523104.1:c.15_21del	XP_011521406.1:p.Tyr6GlyfsTer?
XM_011523105.1:c.15_21del	XP_011521407.1:p.Tyr6GlyfsTer?
XM_011523101.3:c.15_21del	XP_011521403.1:p.Tyr6GlyfsTer?
XM_011523103.3:c.15_21del	XP_011521405.1:p.Tyr6GlyfsTer?
XM_011523104.3:c.15_21del	XP_011521406.1:p.Tyr6GlyfsTer?
XM_011523105.3:c.15_21del	XP_011521407.1:p.Tyr6GlyfsTer?
XM_017023278.2:c.15_21del	XP_016878767.1:p.Tyr6GlyfsTer?
NM_016373.4:c.15_21del MANE Select	NP_057457.1:p.Tyr6GlyfsTer?
NM_001291997.2:c.-260_-254del	NP_001278926.1:n.-260_-254del
NM_130791.4:c.15_21del	NP_570607.1:p.Tyr6GlyfsTer?
NR_120435.2:n.140_146del
NR_120436.2:n.140_146del
NM_130791.5:c.15_21del	NP_570607.1:p.Tyr6GlyfsTer?
NR_120436.3:n.140_146del