Canonical Allele Identifier: CA14329984

Gene: WWOX

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78472009C>T , CM000678.2:g.78472009C>T	GRCh38
NC_000016.9:g.78505906C>T , CM000678.1:g.78505906C>T	GRCh37
NC_000016.8:g.77063407C>T	NCBI36
NG_011698.1:g.377356C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627394.3:c.1056+39257C>T	ENSP00000485925.2:n.1056+39257C>T
ENST00000683929.1:c.1056+39257C>T	ENSP00000507689.1:n.1056+39257C>T
ENST00000684632.1:n.1435+39257C>T
ENST00000566780.6:c.1056+39257C>T MANE Select	ENSP00000457230.1:n.1056+39257C>T
ENST00000402655.6:c.409+356855C>T	ENSP00000384238.2:n.409+356855C>T
ENST00000406884.6:c.516+307720C>T	ENSP00000384495.2:n.516+307720C>T
ENST00000408984.7:c.1056+39257C>T	ENSP00000386161.3:n.1056+39257C>T
ENST00000539474.6:c.410-284931C>T	ENSP00000445210.2:n.410-284931C>T
ENST00000566780.5:c.1056+39257C>T	ENSP00000457230.1:n.1056+39257C>T
ENST00000569332.5:c.*853+39257C>T	ENSP00000454788.1:n.*853+39257C>T
NM_001291997.1:c.717+39257C>T	NP_001278926.1:n.717+39257C>T
NM_016373.3:c.1056+39257C>T	NP_057457.1:n.1056+39257C>T
XM_011523100.1:c.1056+39257C>T	XP_011521402.1:n.1056+39257C>T
XM_011523101.1:c.1056+39257C>T	XP_011521403.1:n.1056+39257C>T
XM_011523102.1:c.1057-27714C>T	XP_011521404.1:n.1057-27714C>T
XM_011523103.1:c.1056+39257C>T	XP_011521405.1:n.1056+39257C>T
XM_011523101.3:c.1056+39257C>T	XP_011521403.1:n.1056+39257C>T
XM_011523103.3:c.1056+39257C>T	XP_011521405.1:n.1056+39257C>T
XM_011523104.3:c.*889C>T	XP_011521406.1:n.*889C>T
NM_016373.4:c.1056+39257C>T MANE Select	NP_057457.1:n.1056+39257C>T
NM_001291997.2:c.717+39257C>T	NP_001278926.1:n.717+39257C>T