Canonical Allele Identifier: CA2234946466

Gene: WWOX

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78224860_78224863delinsCATT , CM000678.2:g.78224860_78224863delinsCATT	GRCh38
NC_000016.9:g.78258757_78258760delinsCATT , CM000678.1:g.78258757_78258760delinsCATT	GRCh37
NC_000016.8:g.76816258_76816261delinsCATT	NCBI36
NG_011698.1:g.130207_130210delinsCATT

Transcript Alleles

HGVS	Amino-acid change
ENST00000627394.3:c.516+60571_516+60574delinsCATT	ENSP00000485925.2:n.516+60571_516+60574delinsCATT
ENST00000683286.1:n.843+60571_843+60574delinsCATT
ENST00000683929.1:c.516+60571_516+60574delinsCATT	ENSP00000507689.1:n.516+60571_516+60574delinsCATT
ENST00000684070.1:n.780+60571_780+60574delinsCATT
ENST00000684632.1:n.895+60571_895+60574delinsCATT
ENST00000566780.6:c.516+60571_516+60574delinsCATT MANE Select	ENSP00000457230.1:n.516+60571_516+60574delinsCATT
ENST00000355860.7:c.517-53743_517-53740delinsCATT	ENSP00000348119.3:n.517-53743_517-53740delinsCATT
ENST00000402655.6:c.409+109706_409+109709delinsCATT	ENSP00000384238.2:n.409+109706_409+109709delinsCATT
ENST00000406884.6:c.516+60571_516+60574delinsCATT	ENSP00000384495.2:n.516+60571_516+60574delinsCATT
ENST00000408984.7:c.516+60571_516+60574delinsCATT	ENSP00000386161.3:n.516+60571_516+60574delinsCATT
ENST00000539474.6:c.409+109706_409+109709delinsCATT	ENSP00000445210.2:n.409+109706_409+109709delinsCATT
ENST00000561846.5:n.561-55981_561-55978delinsCATT
ENST00000562639.5:n.204+60571_204+60574delinsCATT
ENST00000563358.5:n.624-53743_624-53740delinsCATT
ENST00000565791.1:n.204-39609_204-39606delinsCATT
ENST00000566662.5:c.*134+60571_*134+60574delinsCATT	ENSP00000454331.1:n.*134+60571_*134+60574delinsCATT
ENST00000566780.5:c.516+60571_516+60574delinsCATT	ENSP00000457230.1:n.516+60571_516+60574delinsCATT
ENST00000569332.5:c.*313+60571_*313+60574delinsCATT	ENSP00000454788.1:n.*313+60571_*313+60574delinsCATT
ENST00000627394.2:c.*314-53743_*314-53740delinsCATT	ENSP00000485925.1:n.*314-53743_*314-53740delinsCATT
NM_001291997.1:c.177+60571_177+60574delinsCATT	NP_001278926.1:n.177+60571_177+60574delinsCATT
NM_016373.3:c.516+60571_516+60574delinsCATT	NP_057457.1:n.516+60571_516+60574delinsCATT
NM_130791.3:c.517-53743_517-53740delinsCATT	NP_570607.1:n.517-53743_517-53740delinsCATT
NR_120436.1:n.997-53743_997-53740delinsCATT
XM_006721195.2:c.516+60571_516+60574delinsCATT	XP_006721258.1:n.516+60571_516+60574delinsCATT
XM_011523100.1:c.516+60571_516+60574delinsCATT	XP_011521402.1:n.516+60571_516+60574delinsCATT
XM_011523101.1:c.516+60571_516+60574delinsCATT	XP_011521403.1:n.516+60571_516+60574delinsCATT
XM_011523102.1:c.516+60571_516+60574delinsCATT	XP_011521404.1:n.516+60571_516+60574delinsCATT
XM_011523103.1:c.516+60571_516+60574delinsCATT	XP_011521405.1:n.516+60571_516+60574delinsCATT
XM_011523104.1:c.516+60571_516+60574delinsCATT	XP_011521406.1:n.516+60571_516+60574delinsCATT
XM_011523105.1:c.517-3920_517-3917delinsCATT	XP_011521407.1:n.517-3920_517-3917delinsCATT
XM_011523101.3:c.516+60571_516+60574delinsCATT	XP_011521403.1:n.516+60571_516+60574delinsCATT
XM_011523103.3:c.516+60571_516+60574delinsCATT	XP_011521405.1:n.516+60571_516+60574delinsCATT
XM_011523104.3:c.516+60571_516+60574delinsCATT	XP_011521406.1:n.516+60571_516+60574delinsCATT
XM_011523105.3:c.517-3920_517-3917delinsCATT	XP_011521407.1:n.517-3920_517-3917delinsCATT
XM_017023278.2:c.516+60571_516+60574delinsCATT	XP_016878767.1:n.516+60571_516+60574delinsCATT
NM_016373.4:c.516+60571_516+60574delinsCATT MANE Select	NP_057457.1:n.516+60571_516+60574delinsCATT
NM_001291997.2:c.177+60571_177+60574delinsCATT	NP_001278926.1:n.177+60571_177+60574delinsCATT
NM_130791.4:c.517-53743_517-53740delinsCATT	NP_570607.1:n.517-53743_517-53740delinsCATT
NR_120436.2:n.756-53743_756-53740delinsCATT
NM_130791.5:c.517-53743_517-53740delinsCATT	NP_570607.1:n.517-53743_517-53740delinsCATT
NR_120436.3:n.756-53743_756-53740delinsCATT