Canonical Allele Identifier: CA396841607

Gene: WWOX

Linked Data

• MyVariant Identifiers: chr16:g.78198138G>C (hg19) ; chr16:g.78164241G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78164241G>C , CM000678.2:g.78164241G>C	GRCh38
NC_000016.9:g.78198138G>C , CM000678.1:g.78198138G>C	GRCh37
NC_000016.8:g.76755639G>C	NCBI36
NG_011698.1:g.69588G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627394.3:c.468G>C	ENSP00000485925.2:p.Arg156Ser
ENST00000683286.1:n.795G>C
ENST00000683929.1:c.468G>C	ENSP00000507689.1:p.Arg156Ser
ENST00000684070.1:n.732G>C
ENST00000684632.1:n.847G>C
ENST00000566780.6:c.468G>C MANE Select	ENSP00000457230.1:p.Arg156Ser
ENST00000355860.7:c.468G>C	ENSP00000348119.3:p.Arg156Ser
ENST00000402655.6:c.409+49087G>C	ENSP00000384238.2:n.409+49087G>C
ENST00000406884.6:c.468G>C	ENSP00000384495.2:p.Arg156Ser
ENST00000408984.7:c.468G>C	ENSP00000386161.3:p.Arg156Ser
ENST00000539474.6:c.409+49087G>C	ENSP00000445210.2:n.409+49087G>C
ENST00000561846.5:n.512G>C
ENST00000562639.5:n.156G>C
ENST00000563358.5:n.575G>C
ENST00000565791.1:n.76G>C
ENST00000566662.5:c.*86G>C	ENSP00000454331.1:n.*86G>C
ENST00000566780.5:c.468G>C	ENSP00000457230.1:p.Arg156Ser
ENST00000569332.5:c.*265G>C	ENSP00000454788.1:n.*265G>C
ENST00000627394.2:c.*265G>C	ENSP00000485925.1:n.*265G>C
NM_001291997.1:c.129G>C	NP_001278926.1:p.Arg43Ser
NM_016373.3:c.468G>C	NP_057457.1:p.Arg156Ser
NM_130791.3:c.468G>C	NP_570607.1:p.Arg156Ser
NR_120436.1:n.948G>C
XM_006721195.2:c.468G>C	XP_006721258.1:p.Arg156Ser
XM_011523100.1:c.468G>C	XP_011521402.1:p.Arg156Ser
XM_011523101.1:c.468G>C	XP_011521403.1:p.Arg156Ser
XM_011523102.1:c.468G>C	XP_011521404.1:p.Arg156Ser
XM_011523103.1:c.468G>C	XP_011521405.1:p.Arg156Ser
XM_011523104.1:c.468G>C	XP_011521406.1:p.Arg156Ser
XM_011523105.1:c.468G>C	XP_011521407.1:p.Arg156Ser
XM_011523101.3:c.468G>C	XP_011521403.1:p.Arg156Ser
XM_011523103.3:c.468G>C	XP_011521405.1:p.Arg156Ser
XM_011523104.3:c.468G>C	XP_011521406.1:p.Arg156Ser
XM_011523105.3:c.468G>C	XP_011521407.1:p.Arg156Ser
XM_017023278.2:c.468G>C	XP_016878767.1:p.Arg156Ser
NM_016373.4:c.468G>C MANE Select	NP_057457.1:p.Arg156Ser
NM_001291997.2:c.129G>C	NP_001278926.1:p.Arg43Ser
NM_130791.4:c.468G>C	NP_570607.1:p.Arg156Ser
NR_120436.2:n.707G>C
NM_130791.5:c.468G>C	NP_570607.1:p.Arg156Ser
NR_120436.3:n.707G>C