Canonical Allele Identifier: CA396844013

Gene: WWOX

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78386950T>C , CM000678.2:g.78386950T>C	GRCh38
NC_000016.9:g.78420847T>C , CM000678.1:g.78420847T>C	GRCh37
NC_000016.8:g.76978348T>C	NCBI36
NG_011698.1:g.292297T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_016373.4:c.605+2T>C MANE Select	NP_057457.1:n.605+2T>C
ENST00000566780.6:c.605+2T>C MANE Select	ENSP00000457230.1:n.605+2T>C
NM_001291997.1:c.266+2T>C	NP_001278926.1:n.266+2T>C
NM_001291997.2:c.266+2T>C	NP_001278926.1:n.266+2T>C
NM_016373.3:c.605+2T>C	NP_057457.1:n.605+2T>C
ENST00000402655.6:c.409+271796T>C	ENSP00000384238.2:n.409+271796T>C
ENST00000406884.6:c.516+222661T>C	ENSP00000384495.2:n.516+222661T>C
ENST00000408984.7:c.605+2T>C	ENSP00000386161.3:n.605+2T>C
ENST00000539474.6:c.409+271796T>C	ENSP00000445210.2:n.409+271796T>C
ENST00000562639.5:n.293+2T>C
ENST00000566662.5:c.*223+2T>C	ENSP00000454331.1:n.*223+2T>C
ENST00000566780.5:c.605+2T>C	ENSP00000457230.1:n.605+2T>C
ENST00000569332.5:c.*402+2T>C	ENSP00000454788.1:n.*402+2T>C
ENST00000627394.3:c.605+2T>C	ENSP00000485925.2:n.605+2T>C
ENST00000683929.1:c.605+2T>C	ENSP00000507689.1:n.605+2T>C
ENST00000684070.1:n.871T>C
ENST00000684632.1:n.984+2T>C
XM_006721195.2:c.605+2T>C	XP_006721258.1:n.605+2T>C
XM_011523100.1:c.605+2T>C	XP_011521402.1:n.605+2T>C
XM_011523101.1:c.605+2T>C	XP_011521403.1:n.605+2T>C
XM_011523101.3:c.605+2T>C	XP_011521403.1:n.605+2T>C
XM_011523102.1:c.605+2T>C	XP_011521404.1:n.605+2T>C
XM_011523103.1:c.605+2T>C	XP_011521405.1:n.605+2T>C
XM_011523103.3:c.605+2T>C	XP_011521405.1:n.605+2T>C
XM_011523104.1:c.605+2T>C	XP_011521406.1:n.605+2T>C
XM_011523104.3:c.605+2T>C	XP_011521406.1:n.605+2T>C