Canonical Allele Identifier: CA724281606

Gene: WWOX

Linked Data

• dbSNP Id: rs1215141934
• MyVariant Identifiers: chr16:g.78569936G>C (hg19) ; chr16:g.78536039G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78536039G>C , CM000678.2:g.78536039G>C	GRCh38
NC_000016.9:g.78569936G>C , CM000678.1:g.78569936G>C	GRCh37
NC_000016.8:g.77127437G>C	NCBI36
NG_011698.1:g.441386G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627394.3:c.1152+197G>C	ENSP00000485925.2:n.1152+197G>C
ENST00000683929.1:c.1056+103287G>C	ENSP00000507689.1:n.1056+103287G>C
ENST00000684632.1:n.1436-99808G>C
ENST00000566780.6:c.1056+103287G>C MANE Select	ENSP00000457230.1:n.1056+103287G>C
ENST00000402655.6:c.409+420885G>C	ENSP00000384238.2:n.409+420885G>C
ENST00000406884.6:c.516+371750G>C	ENSP00000384495.2:n.516+371750G>C
ENST00000408984.7:c.1056+103287G>C	ENSP00000386161.3:n.1056+103287G>C
ENST00000539474.6:c.410-220901G>C	ENSP00000445210.2:n.410-220901G>C
ENST00000566780.5:c.1056+103287G>C	ENSP00000457230.1:n.1056+103287G>C
ENST00000569332.5:c.*853+103287G>C	ENSP00000454788.1:n.*853+103287G>C
NM_001291997.1:c.717+103287G>C	NP_001278926.1:n.717+103287G>C
NM_016373.3:c.1056+103287G>C	NP_057457.1:n.1056+103287G>C
XM_011523100.1:c.1152+197G>C	XP_011521402.1:n.1152+197G>C
XM_011523101.1:c.1057-38020G>C	XP_011521403.1:n.1057-38020G>C
XM_011523103.1:c.1056+103287G>C	XP_011521405.1:n.1056+103287G>C
XM_011523101.3:c.1057-38020G>C	XP_011521403.1:n.1057-38020G>C
XM_011523103.3:c.1056+103287G>C	XP_011521405.1:n.1056+103287G>C
XM_017023279.1:c.142+197G>C	XP_016878768.1:n.142+197G>C
NM_016373.4:c.1056+103287G>C MANE Select	NP_057457.1:n.1056+103287G>C
NM_001291997.2:c.717+103287G>C	NP_001278926.1:n.717+103287G>C