Canonical Allele Identifier: CA2234905772

Gene: WWOX

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78154739_78154742delinsATAG , CM000678.2:g.78154739_78154742delinsATAG	GRCh38
NC_000016.9:g.78188636_78188639delinsATAG , CM000678.1:g.78188636_78188639delinsATAG	GRCh37
NC_000016.8:g.76746137_76746140delinsATAG	NCBI36
NG_011698.1:g.60086_60089delinsATAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000627394.3:c.410-9444_410-9441delinsATAG	ENSP00000485925.2:n.410-9444_410-9441deli...
ENST00000683286.1:n.737-9444_737-9441delinsATAG
ENST00000683929.1:c.410-9444_410-9441delinsATAG	ENSP00000507689.1:n.410-9444_410-9441deli...
ENST00000684070.1:n.674-9444_674-9441delinsATAG
ENST00000684632.1:n.789-9444_789-9441delinsATAG
ENST00000566780.6:c.410-9444_410-9441delinsATAG MANE Select	ENSP00000457230.1:n.410-9444_410-9441deli...
ENST00000355860.7:c.410-9444_410-9441delinsATAG	ENSP00000348119.3:n.410-9444_410-9441deli...
ENST00000402655.6:c.409+39585_409+39588delinsATAG	ENSP00000384238.2:n.409+39585_409+39588de...
ENST00000406884.6:c.410-9444_410-9441delinsATAG	ENSP00000384495.2:n.410-9444_410-9441deli...
ENST00000408984.7:c.410-9444_410-9441delinsATAG	ENSP00000386161.3:n.410-9444_410-9441deli...
ENST00000539474.6:c.409+39585_409+39588delinsATAG	ENSP00000445210.2:n.409+39585_409+39588de...
ENST00000561846.5:n.454-9444_454-9441delinsATAG
ENST00000562639.5:n.98-9444_98-9441delinsATAG
ENST00000563358.5:n.517-9444_517-9441delinsATAG
ENST00000565791.1:n.17+8806_17+8809delinsATAG
ENST00000566662.5:c.*28-9444_*28-9441delinsATAG	ENSP00000454331.1:n.*28-9444_*28-9441deli...
ENST00000566780.5:c.410-9444_410-9441delinsATAG	ENSP00000457230.1:n.410-9444_410-9441deli...
ENST00000569332.5:c.*207-9444_*207-9441delinsATAG	ENSP00000454788.1:n.*207-9444_*207-9441de...
ENST00000627394.2:c.*207-9444_*207-9441delinsATAG	ENSP00000485925.1:n.*207-9444_*207-9441de...
NM_001291997.1:c.71-9444_71-9441delinsATAG	NP_001278926.1:n.71-9444_71-9441delinsATA...
NM_016373.3:c.410-9444_410-9441delinsATAG	NP_057457.1:n.410-9444_410-9441delinsATAG...
NM_130791.3:c.410-9444_410-9441delinsATAG	NP_570607.1:n.410-9444_410-9441delinsATAG...
NR_120436.1:n.890-9444_890-9441delinsATAG
XM_006721195.2:c.410-9444_410-9441delinsATAG	XP_006721258.1:n.410-9444_410-9441delinsA...
XM_011523100.1:c.410-9444_410-9441delinsATAG	XP_011521402.1:n.410-9444_410-9441delinsA...
XM_011523101.1:c.410-9444_410-9441delinsATAG	XP_011521403.1:n.410-9444_410-9441delinsA...
XM_011523102.1:c.410-9444_410-9441delinsATAG	XP_011521404.1:n.410-9444_410-9441delinsA...
XM_011523103.1:c.410-9444_410-9441delinsATAG	XP_011521405.1:n.410-9444_410-9441delinsA...
XM_011523104.1:c.410-9444_410-9441delinsATAG	XP_011521406.1:n.410-9444_410-9441delinsA...
XM_011523105.1:c.410-9444_410-9441delinsATAG	XP_011521407.1:n.410-9444_410-9441delinsA...
XM_011523101.3:c.410-9444_410-9441delinsATAG	XP_011521403.1:n.410-9444_410-9441delinsA...
XM_011523103.3:c.410-9444_410-9441delinsATAG	XP_011521405.1:n.410-9444_410-9441delinsA...
XM_011523104.3:c.410-9444_410-9441delinsATAG	XP_011521406.1:n.410-9444_410-9441delinsA...
XM_011523105.3:c.410-9444_410-9441delinsATAG	XP_011521407.1:n.410-9444_410-9441delinsA...
XM_017023278.2:c.410-9444_410-9441delinsATAG	XP_016878767.1:n.410-9444_410-9441delinsA...
NM_016373.4:c.410-9444_410-9441delinsATAG MANE Select	NP_057457.1:n.410-9444_410-9441delinsATAG...
NM_001291997.2:c.71-9444_71-9441delinsATAG	NP_001278926.1:n.71-9444_71-9441delinsATA...
NM_130791.4:c.410-9444_410-9441delinsATAG	NP_570607.1:n.410-9444_410-9441delinsATAG...
NR_120436.2:n.649-9444_649-9441delinsATAG
NM_130791.5:c.410-9444_410-9441delinsATAG	NP_570607.1:n.410-9444_410-9441delinsATAG...
NR_120436.3:n.649-9444_649-9441delinsATAG