Canonical Allele Identifier: CA496609387

Gene: WWOX

Linked Data

• gnomAD v4: 16-78099865-C-T
• MyVariant Identifiers: chr16:g.78133762C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78099865C>T , CM000678.2:g.78099865C>T	GRCh38
NC_000016.9:g.78133762C>T , CM000678.1:g.78133762C>T	GRCh37
NC_000016.8:g.76691263C>T	NCBI36
NG_011698.1:g.5212C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627394.3:c.87C>T	ENSP00000485925.2:p.Asp29=
ENST00000682609.1:n.414C>T
ENST00000683286.1:n.414C>T
ENST00000683929.1:c.87C>T	ENSP00000507689.1:p.Asp29=
ENST00000684070.1:n.416C>T
ENST00000684381.1:n.414C>T
ENST00000684452.1:n.414C>T
ENST00000684632.1:n.466C>T
ENST00000566780.6:c.87C>T MANE Select	ENSP00000457230.1:p.Asp29=
ENST00000355860.7:c.87C>T	ENSP00000348119.3:p.Asp29=
ENST00000402655.6:c.87C>T	ENSP00000384238.2:p.Asp29=
ENST00000406884.6:c.87C>T	ENSP00000384495.2:p.Asp29=
ENST00000408984.7:c.87C>T	ENSP00000386161.3:p.Asp29=
ENST00000539474.6:c.87C>T	ENSP00000445210.2:p.Asp29=
ENST00000561846.5:n.131C>T
ENST00000562214.5:n.210C>T
ENST00000563358.5:n.80C>T
ENST00000565562.5:n.132C>T
ENST00000566662.5:c.87C>T	ENSP00000454331.1:p.Asp29=
ENST00000566780.5:c.87C>T	ENSP00000457230.1:p.Asp29=
ENST00000569332.5:c.87C>T	ENSP00000454788.1:p.Asp29=
ENST00000569818.1:c.87C>T	ENSP00000454485.1:p.Asp29=
ENST00000627394.2:c.87C>T	ENSP00000485925.1:p.Asp29=
NM_001291997.1:c.-188C>T	NP_001278926.1:n.-188C>T
NM_016373.3:c.87C>T	NP_057457.1:p.Asp29=
NM_130791.3:c.87C>T	NP_570607.1:p.Asp29=
NR_120435.1:n.453C>T
NR_120436.1:n.453C>T
XM_006721195.2:c.87C>T	XP_006721258.1:p.Asp29=
XM_011523100.1:c.87C>T	XP_011521402.1:p.Asp29=
XM_011523101.1:c.87C>T	XP_011521403.1:p.Asp29=
XM_011523102.1:c.87C>T	XP_011521404.1:p.Asp29=
XM_011523103.1:c.87C>T	XP_011521405.1:p.Asp29=
XM_011523104.1:c.87C>T	XP_011521406.1:p.Asp29=
XM_011523105.1:c.87C>T	XP_011521407.1:p.Asp29=
XM_011523101.3:c.87C>T	XP_011521403.1:p.Asp29=
XM_011523103.3:c.87C>T	XP_011521405.1:p.Asp29=
XM_011523104.3:c.87C>T	XP_011521406.1:p.Asp29=
XM_011523105.3:c.87C>T	XP_011521407.1:p.Asp29=
XM_017023278.2:c.87C>T	XP_016878767.1:p.Asp29=
NM_016373.4:c.87C>T MANE Select	NP_057457.1:p.Asp29=
NM_001291997.2:c.-188C>T	NP_001278926.1:n.-188C>T
NM_130791.4:c.87C>T	NP_570607.1:p.Asp29=
NR_120435.2:n.212C>T
NR_120436.2:n.212C>T
NM_130791.5:c.87C>T	NP_570607.1:p.Asp29=
NR_120436.3:n.212C>T