Canonical Allele Identifier: CA979412818

Gene: WWOX

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78918542A>T , CM000678.2:g.78918542A>T	GRCh38
NC_000016.9:g.78952439A>T , CM000678.1:g.78952439A>T	GRCh37
NC_000016.8:g.77509940A>T	NCBI36
NG_011698.1:g.823889A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683929.1:c.*29-121562A>T	ENSP00000507689.1:n.*29-121562A>T
ENST00000566780.6:c.1057-293066A>T MANE Select	ENSP00000457230.1:n.1057-293066A>T
ENST00000402655.6:c.410-293066A>T	ENSP00000384238.2:n.410-293066A>T
ENST00000406884.6:c.517-293066A>T	ENSP00000384495.2:n.517-293066A>T
ENST00000539474.6:c.485+161527A>T	ENSP00000445210.2:n.485+161527A>T
ENST00000566780.5:c.1057-293066A>T	ENSP00000457230.1:n.1057-293066A>T
ENST00000569332.5:c.*854-293066A>T	ENSP00000454788.1:n.*854-293066A>T
NM_001291997.1:c.718-293066A>T	NP_001278926.1:n.718-293066A>T
NM_016373.3:c.1057-293066A>T	NP_057457.1:n.1057-293066A>T
XM_011523100.1:c.1153-293066A>T	XP_011521402.1:n.1153-293066A>T
XM_011523103.1:c.*28+161527A>T	XP_011521405.1:n.*28+161527A>T
XM_011523103.3:c.*28+161527A>T	XP_011521405.1:n.*28+161527A>T
XM_017023279.1:c.143-293066A>T	XP_016878768.1:n.143-293066A>T
NM_016373.4:c.1057-293066A>T MANE Select	NP_057457.1:n.1057-293066A>T
NM_001291997.2:c.718-293066A>T	NP_001278926.1:n.718-293066A>T