Canonical Allele Identifier: CA2234888863

Gene: WWOX

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78099679_78099680delinsGC , CM000678.2:g.78099679_78099680delinsGC	GRCh38
NC_000016.9:g.78133576_78133577delinsGC , CM000678.1:g.78133576_78133577delinsGC	GRCh37
NC_000016.8:g.76691077_76691078delinsGC	NCBI36
NG_011698.1:g.5026_5027delinsGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000627394.3:c.-100_-99delinsGC	ENSP00000485925.2:n.-100_-99delinsGC
ENST00000682609.1:n.228_229delinsGC
ENST00000683286.1:n.228_229delinsGC
ENST00000683929.1:c.-100_-99delinsGC	ENSP00000507689.1:n.-100_-99delinsGC
ENST00000684070.1:n.230_231delinsGC
ENST00000684381.1:n.228_229delinsGC
ENST00000684452.1:n.228_229delinsGC
ENST00000684632.1:n.280_281delinsGC
ENST00000566780.6:c.-100_-99delinsGC MANE Select	ENSP00000457230.1:n.-100_-99delinsGC
ENST00000355860.7:c.-100_-99delinsGC	ENSP00000348119.3:n.-100_-99delinsGC
ENST00000402655.6:c.-100_-99delinsGC	ENSP00000384238.2:n.-100_-99delinsGC
ENST00000406884.6:c.-100_-99delinsGC	ENSP00000384495.2:n.-100_-99delinsGC
ENST00000539474.6:c.-100_-99delinsGC	ENSP00000445210.2:n.-100_-99delinsGC
ENST00000562214.5:n.24_25delinsGC
ENST00000566662.5:c.-100_-99delinsGC	ENSP00000454331.1:n.-100_-99delinsGC
ENST00000566780.5:c.-100_-99delinsGC	ENSP00000457230.1:n.-100_-99delinsGC
ENST00000569332.5:c.-100_-99delinsGC	ENSP00000454788.1:n.-100_-99delinsGC
ENST00000569818.1:c.-100_-99delinsGC	ENSP00000454485.1:n.-100_-99delinsGC
ENST00000627394.2:c.-100_-99delinsGC	ENSP00000485925.1:n.-100_-99delinsGC
NM_001291997.1:c.-374_-373delinsGC	NP_001278926.1:n.-374_-373delinsGC
NM_016373.3:c.-100_-99delinsGC	NP_057457.1:n.-100_-99delinsGC
NM_130791.3:c.-100_-99delinsGC	NP_570607.1:n.-100_-99delinsGC
NR_120435.1:n.267_268delinsGC
NR_120436.1:n.267_268delinsGC
XM_006721195.2:c.-100_-99delinsGC	XP_006721258.1:n.-100_-99delinsGC
XM_011523100.1:c.-100_-99delinsGC	XP_011521402.1:n.-100_-99delinsGC
XM_011523101.1:c.-100_-99delinsGC	XP_011521403.1:n.-100_-99delinsGC
XM_011523102.1:c.-100_-99delinsGC	XP_011521404.1:n.-100_-99delinsGC
XM_011523103.1:c.-100_-99delinsGC	XP_011521405.1:n.-100_-99delinsGC
XM_011523104.1:c.-100_-99delinsGC	XP_011521406.1:n.-100_-99delinsGC
XM_011523105.1:c.-100_-99delinsGC	XP_011521407.1:n.-100_-99delinsGC
XM_011523101.3:c.-100_-99delinsGC	XP_011521403.1:n.-100_-99delinsGC
XM_011523103.3:c.-100_-99delinsGC	XP_011521405.1:n.-100_-99delinsGC
XM_011523104.3:c.-100_-99delinsGC	XP_011521406.1:n.-100_-99delinsGC
XM_011523105.3:c.-100_-99delinsGC	XP_011521407.1:n.-100_-99delinsGC
XM_017023278.2:c.-100_-99delinsGC	XP_016878767.1:n.-100_-99delinsGC
NM_016373.4:c.-100_-99delinsGC MANE Select	NP_057457.1:n.-100_-99delinsGC
NM_001291997.2:c.-374_-373delinsGC	NP_001278926.1:n.-374_-373delinsGC
NM_130791.4:c.-100_-99delinsGC	NP_570607.1:n.-100_-99delinsGC
NR_120435.2:n.26_27delinsGC
NR_120436.2:n.26_27delinsGC
NM_130791.5:c.-100_-99delinsGC	NP_570607.1:n.-100_-99delinsGC
NR_120436.3:n.26_27delinsGC