Canonical Allele Identifier: CA496609348

Gene: WWOX

Linked Data

• gnomAD v4: 16-78099799-G-C
• MyVariant Identifiers: chr16:g.78133696G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78099799G>C , CM000678.2:g.78099799G>C	GRCh38
NC_000016.9:g.78133696G>C , CM000678.1:g.78133696G>C	GRCh37
NC_000016.8:g.76691197G>C	NCBI36
NG_011698.1:g.5146G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627394.3:c.21G>C	ENSP00000485925.2:p.Ala7=
ENST00000682609.1:n.348G>C
ENST00000683286.1:n.348G>C
ENST00000683929.1:c.21G>C	ENSP00000507689.1:p.Ala7=
ENST00000684070.1:n.350G>C
ENST00000684381.1:n.348G>C
ENST00000684452.1:n.348G>C
ENST00000684632.1:n.400G>C
ENST00000566780.6:c.21G>C MANE Select	ENSP00000457230.1:p.Ala7=
ENST00000355860.7:c.21G>C	ENSP00000348119.3:p.Ala7=
ENST00000402655.6:c.21G>C	ENSP00000384238.2:p.Ala7=
ENST00000406884.6:c.21G>C	ENSP00000384495.2:p.Ala7=
ENST00000408984.7:c.21G>C	ENSP00000386161.3:p.Ala7=
ENST00000539474.6:c.21G>C	ENSP00000445210.2:p.Ala7=
ENST00000561846.5:n.65G>C
ENST00000562214.5:n.144G>C
ENST00000563358.5:n.14G>C
ENST00000565562.5:n.66G>C
ENST00000566662.5:c.21G>C	ENSP00000454331.1:p.Ala7=
ENST00000566780.5:c.21G>C	ENSP00000457230.1:p.Ala7=
ENST00000569332.5:c.21G>C	ENSP00000454788.1:p.Ala7=
ENST00000569818.1:c.21G>C	ENSP00000454485.1:p.Ala7=
ENST00000627394.2:c.21G>C	ENSP00000485925.1:p.Ala7=
NM_001291997.1:c.-254G>C	NP_001278926.1:n.-254G>C
NM_016373.3:c.21G>C	NP_057457.1:p.Ala7=
NM_130791.3:c.21G>C	NP_570607.1:p.Ala7=
NR_120435.1:n.387G>C
NR_120436.1:n.387G>C
XM_006721195.2:c.21G>C	XP_006721258.1:p.Ala7=
XM_011523100.1:c.21G>C	XP_011521402.1:p.Ala7=
XM_011523101.1:c.21G>C	XP_011521403.1:p.Ala7=
XM_011523102.1:c.21G>C	XP_011521404.1:p.Ala7=
XM_011523103.1:c.21G>C	XP_011521405.1:p.Ala7=
XM_011523104.1:c.21G>C	XP_011521406.1:p.Ala7=
XM_011523105.1:c.21G>C	XP_011521407.1:p.Ala7=
XM_011523101.3:c.21G>C	XP_011521403.1:p.Ala7=
XM_011523103.3:c.21G>C	XP_011521405.1:p.Ala7=
XM_011523104.3:c.21G>C	XP_011521406.1:p.Ala7=
XM_011523105.3:c.21G>C	XP_011521407.1:p.Ala7=
XM_017023278.2:c.21G>C	XP_016878767.1:p.Ala7=
NM_016373.4:c.21G>C MANE Select	NP_057457.1:p.Ala7=
NM_001291997.2:c.-254G>C	NP_001278926.1:n.-254G>C
NM_130791.4:c.21G>C	NP_570607.1:p.Ala7=
NR_120435.2:n.146G>C
NR_120436.2:n.146G>C
NM_130791.5:c.21G>C	NP_570607.1:p.Ala7=
NR_120436.3:n.146G>C