Canonical Allele Identifier: CA2235399509

Gene: WWOX

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78829718T= , CM000678.2:g.78829718T=	GRCh38
NC_000016.9:g.78863615T= , CM000678.1:g.78863615T=	GRCh37
NC_000016.8:g.77421116T=	NCBI36
NG_011698.1:g.735065T=

Transcript Alleles

HGVS	Amino-acid Change
NM_016373.4:c.1057-381890T= MANE Select	NP_057457.1:n.1057-381890T=
ENST00000566780.6:c.1057-381890T= MANE Select	ENSP00000457230.1:n.1057-381890T=
NM_001291997.1:c.718-381890T=	NP_001278926.1:n.718-381890T=
NM_001291997.2:c.718-381890T=	NP_001278926.1:n.718-381890T=
NM_016373.3:c.1057-381890T=	NP_057457.1:n.1057-381890T=
ENST00000402655.6:c.410-381890T=	ENSP00000384238.2:n.410-381890T=
ENST00000406884.6:c.517-381890T=	ENSP00000384495.2:n.517-381890T=
ENST00000539474.6:c.485+72703T=	ENSP00000445210.2:n.485+72703T=
ENST00000566780.5:c.1057-381890T=	ENSP00000457230.1:n.1057-381890T=
ENST00000569332.5:c.*854-381890T=	ENSP00000454788.1:n.*854-381890T=
ENST00000683929.1:c.*28+72703T=	ENSP00000507689.1:n.*28+72703T=
XM_011523100.1:c.1152+293876T=	XP_011521402.1:n.1152+293876T=
XM_011523103.1:c.*28+72703T=	XP_011521405.1:n.*28+72703T=
XM_011523103.3:c.*28+72703T=	XP_011521405.1:n.*28+72703T=
XM_017023279.1:c.142+293876T=	XP_016878768.1:n.142+293876T=