Canonical Allele Identifier: CA2235240758

Gene: WWOX

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78624496T= , CM000678.2:g.78624496T=	GRCh38
NC_000016.9:g.78658393T= , CM000678.1:g.78658393T=	GRCh37
NC_000016.8:g.77215894T=	NCBI36
NG_011698.1:g.529843T=

Transcript Alleles

HGVS	Amino-acid Change
NM_016373.4:c.1056+191744T= MANE Select	NP_057457.1:n.1056+191744T=
ENST00000566780.6:c.1056+191744T= MANE Select	ENSP00000457230.1:n.1056+191744T=
NM_001291997.1:c.717+191744T=	NP_001278926.1:n.717+191744T=
NM_001291997.2:c.717+191744T=	NP_001278926.1:n.717+191744T=
NM_016373.3:c.1056+191744T=	NP_057457.1:n.1056+191744T=
ENST00000402655.6:c.409+509342T=	ENSP00000384238.2:n.409+509342T=
ENST00000406884.6:c.516+460207T=	ENSP00000384495.2:n.516+460207T=
ENST00000408984.7:c.1057-66746T=	ENSP00000386161.3:n.1057-66746T=
ENST00000539474.6:c.410-132444T=	ENSP00000445210.2:n.410-132444T=
ENST00000566780.5:c.1056+191744T=	ENSP00000457230.1:n.1056+191744T=
ENST00000569332.5:c.*853+191744T=	ENSP00000454788.1:n.*853+191744T=
ENST00000683929.1:c.1057-132444T=	ENSP00000507689.1:n.1057-132444T=
ENST00000684632.1:n.1436-11351T=
XM_011523100.1:c.1152+88654T=	XP_011521402.1:n.1152+88654T=
XM_011523103.1:c.1057-132444T=	XP_011521405.1:n.1057-132444T=
XM_011523103.3:c.1057-132444T=	XP_011521405.1:n.1057-132444T=
XM_017023279.1:c.142+88654T=	XP_016878768.1:n.142+88654T=