Canonical Allele Identifier: CA2235147042

Gene: WWOX

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78536010C= , CM000678.2:g.78536010C=	GRCh38
NC_000016.9:g.78569907C= , CM000678.1:g.78569907C=	GRCh37
NC_000016.8:g.77127408C=	NCBI36
NG_011698.1:g.441357C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627394.3:c.1152+168C=	ENSP00000485925.2:n.1152+168C=
ENST00000683929.1:c.1056+103258C=	ENSP00000507689.1:n.1056+103258C=
ENST00000684632.1:n.1436-99837C=
ENST00000566780.6:c.1056+103258C= MANE Select	ENSP00000457230.1:n.1056+103258C=
ENST00000402655.6:c.409+420856C=	ENSP00000384238.2:n.409+420856C=
ENST00000406884.6:c.516+371721C=	ENSP00000384495.2:n.516+371721C=
ENST00000408984.7:c.1056+103258C=	ENSP00000386161.3:n.1056+103258C=
ENST00000539474.6:c.410-220930C=	ENSP00000445210.2:n.410-220930C=
ENST00000566780.5:c.1056+103258C=	ENSP00000457230.1:n.1056+103258C=
ENST00000569332.5:c.*853+103258C=	ENSP00000454788.1:n.*853+103258C=
NM_001291997.1:c.717+103258C=	NP_001278926.1:n.717+103258C=
NM_016373.3:c.1056+103258C=	NP_057457.1:n.1056+103258C=
XM_011523100.1:c.1152+168C=	XP_011521402.1:n.1152+168C=
XM_011523101.1:c.1057-38049C=	XP_011521403.1:n.1057-38049C=
XM_011523103.1:c.1056+103258C=	XP_011521405.1:n.1056+103258C=
XM_011523101.3:c.1057-38049C=	XP_011521403.1:n.1057-38049C=
XM_011523103.3:c.1056+103258C=	XP_011521405.1:n.1056+103258C=
XM_017023279.1:c.142+168C=	XP_016878768.1:n.142+168C=
NM_016373.4:c.1056+103258C= MANE Select	NP_057457.1:n.1056+103258C=
NM_001291997.2:c.717+103258C=	NP_001278926.1:n.717+103258C=