Canonical Allele Identifier: CA284493646

Gene: WWOX

Linked Data

• dbSNP Id: rs539488767
• gnomAD v3: 16-78153056-G-T
• gnomAD v4: 16-78153056-G-T
• MyVariant Identifiers: chr16:g.78186953G>T (hg19) ; chr16:g.78153056G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78153056G>T , CM000678.2:g.78153056G>T	GRCh38
NC_000016.9:g.78186953G>T , CM000678.1:g.78186953G>T	GRCh37
NC_000016.8:g.76744454G>T	NCBI36
NG_011698.1:g.58403G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627394.3:c.410-11127G>T	ENSP00000485925.2:n.410-11127G>T
ENST00000683286.1:n.737-11127G>T
ENST00000683929.1:c.410-11127G>T	ENSP00000507689.1:n.410-11127G>T
ENST00000684070.1:n.674-11127G>T
ENST00000684632.1:n.789-11127G>T
ENST00000566780.6:c.410-11127G>T MANE Select	ENSP00000457230.1:n.410-11127G>T
ENST00000355860.7:c.410-11127G>T	ENSP00000348119.3:n.410-11127G>T
ENST00000402655.6:c.409+37902G>T	ENSP00000384238.2:n.409+37902G>T
ENST00000406884.6:c.410-11127G>T	ENSP00000384495.2:n.410-11127G>T
ENST00000408984.7:c.410-11127G>T	ENSP00000386161.3:n.410-11127G>T
ENST00000539474.6:c.409+37902G>T	ENSP00000445210.2:n.409+37902G>T
ENST00000561846.5:n.454-11127G>T
ENST00000562639.5:n.98-11127G>T
ENST00000563358.5:n.517-11127G>T
ENST00000565791.1:n.17+7123G>T
ENST00000566662.5:c.*28-11127G>T	ENSP00000454331.1:n.*28-11127G>T
ENST00000566780.5:c.410-11127G>T	ENSP00000457230.1:n.410-11127G>T
ENST00000569332.5:c.*207-11127G>T	ENSP00000454788.1:n.*207-11127G>T
ENST00000627394.2:c.*207-11127G>T	ENSP00000485925.1:n.*207-11127G>T
NM_001291997.1:c.71-11127G>T	NP_001278926.1:n.71-11127G>T
NM_016373.3:c.410-11127G>T	NP_057457.1:n.410-11127G>T
NM_130791.3:c.410-11127G>T	NP_570607.1:n.410-11127G>T
NR_120436.1:n.890-11127G>T
XM_006721195.2:c.410-11127G>T	XP_006721258.1:n.410-11127G>T
XM_011523100.1:c.410-11127G>T	XP_011521402.1:n.410-11127G>T
XM_011523101.1:c.410-11127G>T	XP_011521403.1:n.410-11127G>T
XM_011523102.1:c.410-11127G>T	XP_011521404.1:n.410-11127G>T
XM_011523103.1:c.410-11127G>T	XP_011521405.1:n.410-11127G>T
XM_011523104.1:c.410-11127G>T	XP_011521406.1:n.410-11127G>T
XM_011523105.1:c.410-11127G>T	XP_011521407.1:n.410-11127G>T
XM_011523101.3:c.410-11127G>T	XP_011521403.1:n.410-11127G>T
XM_011523103.3:c.410-11127G>T	XP_011521405.1:n.410-11127G>T
XM_011523104.3:c.410-11127G>T	XP_011521406.1:n.410-11127G>T
XM_011523105.3:c.410-11127G>T	XP_011521407.1:n.410-11127G>T
XM_017023278.2:c.410-11127G>T	XP_016878767.1:n.410-11127G>T
NM_016373.4:c.410-11127G>T MANE Select	NP_057457.1:n.410-11127G>T
NM_001291997.2:c.71-11127G>T	NP_001278926.1:n.71-11127G>T
NM_130791.4:c.410-11127G>T	NP_570607.1:n.410-11127G>T
NR_120436.2:n.649-11127G>T
NM_130791.5:c.410-11127G>T	NP_570607.1:n.410-11127G>T
NR_120436.3:n.649-11127G>T