Canonical Allele Identifier: CA2235147024

Gene: WWOX

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78535996T= , CM000678.2:g.78535996T=	GRCh38
NC_000016.9:g.78569893T= , CM000678.1:g.78569893T=	GRCh37
NC_000016.8:g.77127394T=	NCBI36
NG_011698.1:g.441343T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627394.3:c.1152+154T=	ENSP00000485925.2:n.1152+154T=
ENST00000683929.1:c.1056+103244T=	ENSP00000507689.1:n.1056+103244T=
ENST00000684632.1:n.1436-99851T=
ENST00000566780.6:c.1056+103244T= MANE Select	ENSP00000457230.1:n.1056+103244T=
ENST00000402655.6:c.409+420842T=	ENSP00000384238.2:n.409+420842T=
ENST00000406884.6:c.516+371707T=	ENSP00000384495.2:n.516+371707T=
ENST00000408984.7:c.1056+103244T=	ENSP00000386161.3:n.1056+103244T=
ENST00000539474.6:c.410-220944T=	ENSP00000445210.2:n.410-220944T=
ENST00000566780.5:c.1056+103244T=	ENSP00000457230.1:n.1056+103244T=
ENST00000569332.5:c.*853+103244T=	ENSP00000454788.1:n.*853+103244T=
NM_001291997.1:c.717+103244T=	NP_001278926.1:n.717+103244T=
NM_016373.3:c.1056+103244T=	NP_057457.1:n.1056+103244T=
XM_011523100.1:c.1152+154T=	XP_011521402.1:n.1152+154T=
XM_011523101.1:c.1057-38063T=	XP_011521403.1:n.1057-38063T=
XM_011523103.1:c.1056+103244T=	XP_011521405.1:n.1056+103244T=
XM_011523101.3:c.1057-38063T=	XP_011521403.1:n.1057-38063T=
XM_011523103.3:c.1056+103244T=	XP_011521405.1:n.1056+103244T=
XM_017023279.1:c.142+154T=	XP_016878768.1:n.142+154T=
NM_016373.4:c.1056+103244T= MANE Select	NP_057457.1:n.1056+103244T=
NM_001291997.2:c.717+103244T=	NP_001278926.1:n.717+103244T=