Canonical Allele Identifier: CA2235530353

Gene: WWOX

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.79039524C>A , CM000678.2:g.79039524C>A	GRCh38
NC_000016.9:g.79073421C>A , CM000678.1:g.79073421C>A	GRCh37
NC_000016.8:g.77630922C>A	NCBI36
NG_011698.1:g.944871C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683929.1:c.*29-580C>A	ENSP00000507689.1:n.*29-580C>A
ENST00000566780.6:c.1057-172084C>A MANE Select	ENSP00000457230.1:n.1057-172084C>A
ENST00000402655.6:c.410-172084C>A	ENSP00000384238.2:n.410-172084C>A
ENST00000406884.6:c.517-172084C>A	ENSP00000384495.2:n.517-172084C>A
ENST00000539474.6:c.486-172084C>A	ENSP00000445210.2:n.486-172084C>A
ENST00000566780.5:c.1057-172084C>A	ENSP00000457230.1:n.1057-172084C>A
ENST00000569332.5:c.*854-172084C>A	ENSP00000454788.1:n.*854-172084C>A
NM_001291997.1:c.718-172084C>A	NP_001278926.1:n.718-172084C>A
NM_016373.3:c.1057-172084C>A	NP_057457.1:n.1057-172084C>A
XM_011523100.1:c.1153-172084C>A	XP_011521402.1:n.1153-172084C>A
XM_011523103.1:c.*29-172084C>A	XP_011521405.1:n.*29-172084C>A
XM_011523103.3:c.*29-172084C>A	XP_011521405.1:n.*29-172084C>A
XM_017023279.1:c.143-172084C>A	XP_016878768.1:n.143-172084C>A
NM_016373.4:c.1057-172084C>A MANE Select	NP_057457.1:n.1057-172084C>A
NM_001291997.2:c.718-172084C>A	NP_001278926.1:n.718-172084C>A