Canonical Allele Identifier: CA2235072759
Gene: WWOX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.78432538C= , CM000678.2:g.78432538C= GRCh38
NC_000016.9:g.78466435C= , CM000678.1:g.78466435C= GRCh37
NC_000016.8:g.77023936C= NCBI36
NG_011698.1:g.337885C=

Transcript Alleles

HGVS Amino-acid change
ENST00000627394.3:c.842C= ENSP00000485925.2:p.Ser281=
ENST00000683929.1:c.842C= ENSP00000507689.1:p.Ser281=
ENST00000684632.1:n.1221C=
ENST00000566780.6:c.842C= MANE Select ENSP00000457230.1:p.Ser281=
ENST00000402655.6:c.409+317384C= ENSP00000384238.2:n.409+317384C=
ENST00000406884.6:c.516+268249C= ENSP00000384495.2:n.516+268249C=
ENST00000408984.7:c.842C= ENSP00000386161.3:p.Ser281=
ENST00000539474.6:c.409+317384C= ENSP00000445210.2:n.409+317384C=
ENST00000562639.5:n.530C=
ENST00000566780.5:c.842C= ENSP00000457230.1:p.Ser281=
ENST00000569332.5:c.*639C= ENSP00000454788.1:n.*639C=
ENST00000620008.1:c.236C= ENSP00000482648.1:p.Ser79=
NM_001291997.1:c.503C= NP_001278926.1:p.Ser168=
NM_016373.3:c.842C= NP_057457.1:p.Ser281=
XM_006721195.2:c.842C= XP_006721258.1:p.Ser281=
XM_011523100.1:c.842C= XP_011521402.1:p.Ser281=
XM_011523101.1:c.842C= XP_011521403.1:p.Ser281=
XM_011523102.1:c.842C= XP_011521404.1:p.Ser281=
XM_011523103.1:c.842C= XP_011521405.1:p.Ser281=
XM_011523104.1:c.842C= XP_011521406.1:p.Ser281=
XR_933765.1:n.3419-1725G=
XM_011523101.3:c.842C= XP_011521403.1:p.Ser281=
XM_011523103.3:c.842C= XP_011521405.1:p.Ser281=
XM_011523104.3:c.842C= XP_011521406.1:p.Ser281=
NM_016373.4:c.842C= MANE Select NP_057457.1:p.Ser281=
NM_001291997.2:c.503C= NP_001278926.1:p.Ser168=