Canonical Allele Identifier: CA8183884

Gene: WWOX MAF

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.79212001_79212005del , CM000678.2:g.79212001_79212005del	GRCh38
NC_000016.9:g.79245898_79245902del , CM000678.1:g.79245898_79245902del	GRCh37
NC_000016.8:g.77803399_77803403del	NCBI36
NG_011698.1:g.1117348_1117352del

Transcript Alleles

HGVS	Amino-acid Change
NM_016373.4:c.*205_*209del (WWOX) MANE Select	NP_057457.1:n.*205_*209del
ENST00000566780.6:c.*205_*209del (WWOX) MANE Select	ENSP00000457230.1:n.*205_*209del
NM_001291997.1:c.*205_*209del (WWOX)	NP_001278926.1:n.*205_*209del
NM_001291997.2:c.*205_*209del (WWOX)	NP_001278926.1:n.*205_*209del
NM_016373.3:c.*205_*209del (WWOX)	NP_057457.1:n.*205_*209del
ENST00000402655.6:c.803_807del (WWOX)	ENSP00000384238.2:p.Trp268Ter
ENST00000406884.6:c.*205_*209del (WWOX)	ENSP00000384495.2:n.*205_*209del
ENST00000539474.6:c.*237_*241del (WWOX)	ENSP00000445210.2:n.*237_*241del
ENST00000566103.1:n.517_521del (WWOX)
ENST00000566780.5:c.*205_*209del (WWOX)	ENSP00000457230.1:n.*205_*209del
ENST00000569332.5:c.*1247_*1251del (WWOX)	ENSP00000454788.1:n.*1247_*1251del
ENST00000683929.1:c.*564_*568del (WWOX)	ENSP00000507689.1:n.*564_*568del
XM_011523100.1:c.*205_*209del (WWOX)	XP_011521402.1:n.*205_*209del
XM_011523103.3:c.*422_*426del (WWOX)	XP_011521405.1:n.*422_*426del
XM_017023279.1:c.536_540del (WWOX)	XP_016878768.1:p.Trp179Ter
XM_024450279.1:c.*930_*934del (MAF)	XP_024306047.1:n.*930_*934del
XR_001751902.2:n.4132_4136del (MAF)
XR_002957802.1:n.4132_4136del (MAF)
XR_002957803.1:n.4132_4136del (MAF)
XR_002957804.1:n.4132_4136del (MAF)