Canonical Allele Identifier: CA623626031

Gene: WWOX

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78386622_78386623insCCCCCCC , CM000678.2:g.78386622_78386623insCCCCCCC	GRCh38
NC_000016.9:g.78420519_78420520insCCCCCCC , CM000678.1:g.78420519_78420520insCCCCCCC	GRCh37
NC_000016.8:g.76978020_76978021insCCCCCCC	NCBI36
NG_011698.1:g.291969_291970insCCCCCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627394.3:c.517-238_517-237insCCCCCCC	ENSP00000485925.2:n.517-238_517-237insCCCCCCC
ENST00000683929.1:c.517-238_517-237insCCCCCCC	ENSP00000507689.1:n.517-238_517-237insCCCCCCC
ENST00000684070.1:n.781-238_781-237insCCCCCCC
ENST00000684632.1:n.896-238_896-237insCCCCCCC
ENST00000566780.6:c.517-238_517-237insCCCCCCC MANE Select	ENSP00000457230.1:n.517-238_517-237insCCCCCCC
ENST00000402655.6:c.409+271468_409+271469insCCCCCCC	ENSP00000384238.2:n.409+271468_409+271469insCCCCCCC
ENST00000406884.6:c.516+222333_516+222334insCCCCCCC	ENSP00000384495.2:n.516+222333_516+222334insCCCCCCC
ENST00000408984.7:c.517-238_517-237insCCCCCCC	ENSP00000386161.3:n.517-238_517-237insCCCCCCC
ENST00000539474.6:c.409+271468_409+271469insCCCCCCC	ENSP00000445210.2:n.409+271468_409+271469insCCCCCCC
ENST00000562639.5:n.205-238_205-237insCCCCCCC
ENST00000566662.5:c.*135-238_*135-237insCCCCCCC	ENSP00000454331.1:n.*135-238_*135-237insCCCCCCC
ENST00000566780.5:c.517-238_517-237insCCCCCCC	ENSP00000457230.1:n.517-238_517-237insCCCCCCC
ENST00000569332.5:c.*314-238_*314-237insCCCCCCC	ENSP00000454788.1:n.*314-238_*314-237insCCCCCCC
NM_001291997.1:c.178-238_178-237insCCCCCCC	NP_001278926.1:n.178-238_178-237insCCCCCCC
NM_016373.3:c.517-238_517-237insCCCCCCC	NP_057457.1:n.517-238_517-237insCCCCCCC
XM_006721195.2:c.517-238_517-237insCCCCCCC	XP_006721258.1:n.517-238_517-237insCCCCCCC
XM_011523100.1:c.517-238_517-237insCCCCCCC	XP_011521402.1:n.517-238_517-237insCCCCCCC
XM_011523101.1:c.517-238_517-237insCCCCCCC	XP_011521403.1:n.517-238_517-237insCCCCCCC
XM_011523102.1:c.517-238_517-237insCCCCCCC	XP_011521404.1:n.517-238_517-237insCCCCCCC
XM_011523103.1:c.517-238_517-237insCCCCCCC	XP_011521405.1:n.517-238_517-237insCCCCCCC
XM_011523104.1:c.517-238_517-237insCCCCCCC	XP_011521406.1:n.517-238_517-237insCCCCCCC
XM_011523101.3:c.517-238_517-237insCCCCCCC	XP_011521403.1:n.517-238_517-237insCCCCCCC
XM_011523103.3:c.517-238_517-237insCCCCCCC	XP_011521405.1:n.517-238_517-237insCCCCCCC
XM_011523104.3:c.517-238_517-237insCCCCCCC	XP_011521406.1:n.517-238_517-237insCCCCCCC
NM_016373.4:c.517-238_517-237insCCCCCCC MANE Select	NP_057457.1:n.517-238_517-237insCCCCCCC
NM_001291997.2:c.178-238_178-237insCCCCCCC	NP_001278926.1:n.178-238_178-237insCCCCCCC