Canonical Allele Identifier: CA284567581

Gene: WWOX

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78386887C>G , CM000678.2:g.78386887C>G	GRCh38
NC_000016.9:g.78420784C>G , CM000678.1:g.78420784C>G	GRCh37
NC_000016.8:g.76978285C>G	NCBI36
NG_011698.1:g.292234C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_016373.4:c.544C>G MANE Select	NP_057457.1:p.Leu182Val
ENST00000566780.6:c.544C>G MANE Select	ENSP00000457230.1:p.Leu182Val
NM_001291997.1:c.205C>G	NP_001278926.1:p.Leu69Val
NM_001291997.2:c.205C>G	NP_001278926.1:p.Leu69Val
NM_016373.3:c.544C>G	NP_057457.1:p.Leu182Val
ENST00000402655.6:c.409+271733C>G	ENSP00000384238.2:n.409+271733C>G
ENST00000406884.6:c.516+222598C>G	ENSP00000384495.2:n.516+222598C>G
ENST00000408984.7:c.544C>G	ENSP00000386161.3:p.Leu182Val
ENST00000539474.6:c.409+271733C>G	ENSP00000445210.2:n.409+271733C>G
ENST00000562639.5:n.232C>G
ENST00000566662.5:c.*162C>G	ENSP00000454331.1:n.*162C>G
ENST00000566780.5:c.544C>G	ENSP00000457230.1:p.Leu182Val
ENST00000569332.5:c.*341C>G	ENSP00000454788.1:n.*341C>G
ENST00000627394.3:c.544C>G	ENSP00000485925.2:p.Leu182Val
ENST00000683929.1:c.544C>G	ENSP00000507689.1:p.Leu182Val
ENST00000684070.1:n.808C>G
ENST00000684632.1:n.923C>G
XM_006721195.2:c.544C>G	XP_006721258.1:p.Leu182Val
XM_011523100.1:c.544C>G	XP_011521402.1:p.Leu182Val
XM_011523101.1:c.544C>G	XP_011521403.1:p.Leu182Val
XM_011523101.3:c.544C>G	XP_011521403.1:p.Leu182Val
XM_011523102.1:c.544C>G	XP_011521404.1:p.Leu182Val
XM_011523103.1:c.544C>G	XP_011521405.1:p.Leu182Val
XM_011523103.3:c.544C>G	XP_011521405.1:p.Leu182Val
XM_011523104.1:c.544C>G	XP_011521406.1:p.Leu182Val
XM_011523104.3:c.544C>G	XP_011521406.1:p.Leu182Val