Canonical Allele Identifier: CA496609441

Gene: WWOX

Linked Data

• MyVariant Identifiers: chr16:g.78142326C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78108429C>A , CM000678.2:g.78108429C>A	GRCh38
NC_000016.9:g.78142326C>A , CM000678.1:g.78142326C>A	GRCh37
NC_000016.8:g.76699827C>A	NCBI36
NG_011698.1:g.13776C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627394.3:c.114C>A	ENSP00000485925.2:p.Thr38=
ENST00000682609.1:n.441C>A
ENST00000683286.1:n.441C>A
ENST00000683929.1:c.114C>A	ENSP00000507689.1:p.Thr38=
ENST00000684070.1:n.437-1349C>A
ENST00000684381.1:n.441C>A
ENST00000684452.1:n.441C>A
ENST00000684632.1:n.493C>A
ENST00000566780.6:c.114C>A MANE Select	ENSP00000457230.1:p.Thr38=
ENST00000355860.7:c.114C>A	ENSP00000348119.3:p.Thr38=
ENST00000402655.6:c.114C>A	ENSP00000384238.2:p.Thr38=
ENST00000406884.6:c.114C>A	ENSP00000384495.2:p.Thr38=
ENST00000408984.7:c.114C>A	ENSP00000386161.3:p.Thr38=
ENST00000539474.6:c.114C>A	ENSP00000445210.2:p.Thr38=
ENST00000561846.5:n.158C>A
ENST00000562214.5:n.237C>A
ENST00000563358.5:n.221C>A
ENST00000565562.5:n.159C>A
ENST00000566662.5:c.108-1349C>A	ENSP00000454331.1:n.108-1349C>A
ENST00000566780.5:c.114C>A	ENSP00000457230.1:p.Thr38=
ENST00000569332.5:c.108-1349C>A	ENSP00000454788.1:n.108-1349C>A
ENST00000627394.2:c.108-1349C>A	ENSP00000485925.1:n.108-1349C>A
NM_001291997.1:c.-167-1349C>A	NP_001278926.1:n.-167-1349C>A
NM_016373.3:c.114C>A	NP_057457.1:p.Thr38=
NM_130791.3:c.114C>A	NP_570607.1:p.Thr38=
NR_120436.1:n.594C>A
XM_006721195.2:c.114C>A	XP_006721258.1:p.Thr38=
XM_011523100.1:c.114C>A	XP_011521402.1:p.Thr38=
XM_011523101.1:c.114C>A	XP_011521403.1:p.Thr38=
XM_011523102.1:c.114C>A	XP_011521404.1:p.Thr38=
XM_011523103.1:c.114C>A	XP_011521405.1:p.Thr38=
XM_011523104.1:c.114C>A	XP_011521406.1:p.Thr38=
XM_011523105.1:c.114C>A	XP_011521407.1:p.Thr38=
XM_011523101.3:c.114C>A	XP_011521403.1:p.Thr38=
XM_011523103.3:c.114C>A	XP_011521405.1:p.Thr38=
XM_011523104.3:c.114C>A	XP_011521406.1:p.Thr38=
XM_011523105.3:c.114C>A	XP_011521407.1:p.Thr38=
XM_017023278.2:c.114C>A	XP_016878767.1:p.Thr38=
NM_016373.4:c.114C>A MANE Select	NP_057457.1:p.Thr38=
NM_001291997.2:c.-167-1349C>A	NP_001278926.1:n.-167-1349C>A
NM_130791.4:c.114C>A	NP_570607.1:p.Thr38=
NR_120436.2:n.353C>A
NM_130791.5:c.114C>A	NP_570607.1:p.Thr38=
NR_120436.3:n.353C>A