Canonical Allele Identifier: CA724268100

Gene: WWOX

Linked Data

• ClinVar Variation Id: 1635062
• ClinVar RCV Id: RCV002133176
• dbSNP Id: rs1313734754
• gnomAD v3: 16-78099901-T-G
• gnomAD v4: 16-78099901-T-G
• MyVariant Identifiers: chr16:g.78133798T>G (hg19) ; chr16:g.78099901T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78099901T>G , CM000678.2:g.78099901T>G	GRCh38
NC_000016.9:g.78133798T>G , CM000678.1:g.78133798T>G	GRCh37
NC_000016.8:g.76691299T>G	NCBI36
NG_011698.1:g.5248T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627394.3:c.107+16T>G	ENSP00000485925.2:n.107+16T>G
ENST00000682609.1:n.434+16T>G
ENST00000683286.1:n.434+16T>G
ENST00000683929.1:c.107+16T>G	ENSP00000507689.1:n.107+16T>G
ENST00000684070.1:n.436+16T>G
ENST00000684381.1:n.434+16T>G
ENST00000684452.1:n.434+16T>G
ENST00000684632.1:n.486+16T>G
ENST00000566780.6:c.107+16T>G MANE Select	ENSP00000457230.1:n.107+16T>G
ENST00000355860.7:c.107+16T>G	ENSP00000348119.3:n.107+16T>G
ENST00000402655.6:c.107+16T>G	ENSP00000384238.2:n.107+16T>G
ENST00000406884.6:c.107+16T>G	ENSP00000384495.2:n.107+16T>G
ENST00000408984.7:c.107+16T>G	ENSP00000386161.3:n.107+16T>G
ENST00000539474.6:c.107+16T>G	ENSP00000445210.2:n.107+16T>G
ENST00000561846.5:n.151+16T>G
ENST00000562214.5:n.230+16T>G
ENST00000563358.5:n.116T>G
ENST00000565562.5:n.152+16T>G
ENST00000566662.5:c.107+16T>G	ENSP00000454331.1:n.107+16T>G
ENST00000566780.5:c.107+16T>G	ENSP00000457230.1:n.107+16T>G
ENST00000569332.5:c.107+16T>G	ENSP00000454788.1:n.107+16T>G
ENST00000569818.1:c.*12T>G	ENSP00000454485.1:n.*12T>G
ENST00000627394.2:c.107+16T>G	ENSP00000485925.1:n.107+16T>G
NM_001291997.1:c.-168+16T>G	NP_001278926.1:n.-168+16T>G
NM_016373.3:c.107+16T>G	NP_057457.1:n.107+16T>G
NM_130791.3:c.107+16T>G	NP_570607.1:n.107+16T>G
NR_120435.1:n.489T>G
NR_120436.1:n.489T>G
XM_006721195.2:c.107+16T>G	XP_006721258.1:n.107+16T>G
XM_011523100.1:c.107+16T>G	XP_011521402.1:n.107+16T>G
XM_011523101.1:c.107+16T>G	XP_011521403.1:n.107+16T>G
XM_011523102.1:c.107+16T>G	XP_011521404.1:n.107+16T>G
XM_011523103.1:c.107+16T>G	XP_011521405.1:n.107+16T>G
XM_011523104.1:c.107+16T>G	XP_011521406.1:n.107+16T>G
XM_011523105.1:c.107+16T>G	XP_011521407.1:n.107+16T>G
XM_011523101.3:c.107+16T>G	XP_011521403.1:n.107+16T>G
XM_011523103.3:c.107+16T>G	XP_011521405.1:n.107+16T>G
XM_011523104.3:c.107+16T>G	XP_011521406.1:n.107+16T>G
XM_011523105.3:c.107+16T>G	XP_011521407.1:n.107+16T>G
XM_017023278.2:c.107+16T>G	XP_016878767.1:n.107+16T>G
NM_016373.4:c.107+16T>G MANE Select	NP_057457.1:n.107+16T>G
NM_001291997.2:c.-168+16T>G	NP_001278926.1:n.-168+16T>G
NM_130791.4:c.107+16T>G	NP_570607.1:n.107+16T>G
NR_120435.2:n.248T>G
NR_120436.2:n.248T>G
NM_130791.5:c.107+16T>G	NP_570607.1:n.107+16T>G
NR_120436.3:n.248T>G