Canonical Allele Identifier: CA2235637961

Gene: WWOX

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.79134048A>C , CM000678.2:g.79134048A>C	GRCh38
NC_000016.9:g.79167945A>C , CM000678.1:g.79167945A>C	GRCh37
NC_000016.8:g.77725446A>C	NCBI36
NG_011698.1:g.1039395A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683929.1:c.*171-77560A>C	ENSP00000507689.1:n.*171-77560A>C
ENST00000566780.6:c.1057-77560A>C MANE Select	ENSP00000457230.1:n.1057-77560A>C
ENST00000402655.6:c.410-77560A>C	ENSP00000384238.2:n.410-77560A>C
ENST00000406884.6:c.517-77560A>C	ENSP00000384495.2:n.517-77560A>C
ENST00000539474.6:c.486-77560A>C	ENSP00000445210.2:n.486-77560A>C
ENST00000566780.5:c.1057-77560A>C	ENSP00000457230.1:n.1057-77560A>C
ENST00000569332.5:c.*854-77560A>C	ENSP00000454788.1:n.*854-77560A>C
NM_001291997.1:c.718-77560A>C	NP_001278926.1:n.718-77560A>C
NM_016373.3:c.1057-77560A>C	NP_057457.1:n.1057-77560A>C
XM_011523100.1:c.1153-77560A>C	XP_011521402.1:n.1153-77560A>C
XM_011523103.1:c.*29-77560A>C	XP_011521405.1:n.*29-77560A>C
XM_011523103.3:c.*29-77560A>C	XP_011521405.1:n.*29-77560A>C
XM_017023279.1:c.143-77560A>C	XP_016878768.1:n.143-77560A>C
NM_016373.4:c.1057-77560A>C MANE Select	NP_057457.1:n.1057-77560A>C
NM_001291997.2:c.718-77560A>C	NP_001278926.1:n.718-77560A>C