Canonical Allele Identifier: CA2573152724

Gene: WWOX MAF

Linked Data

• ClinVar Variation Id: 1661153
• ClinVar RCV Id: RCV002190817
• dbSNP Id: rs2150867224

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.79211586_79211588del , CM000678.2:g.79211586_79211588del	GRCh38
NC_000016.9:g.79245483_79245485del , CM000678.1:g.79245483_79245485del	GRCh37
NC_000016.8:g.77802984_77802986del	NCBI36
NG_011698.1:g.1116933_1116935del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683929.1:c.*171-22_*171-20del (WWOX)	ENSP00000507689.1:n.*171-22_*171-20del
ENST00000566780.6:c.1057-22_1057-20del (WWOX) MANE Select	ENSP00000457230.1:n.1057-22_1057-20del
ENST00000402655.6:c.410-22_410-20del (WWOX)	ENSP00000384238.2:n.410-22_410-20del
ENST00000406884.6:c.517-22_517-20del (WWOX)	ENSP00000384495.2:n.517-22_517-20del
ENST00000539474.6:c.486-22_486-20del (WWOX)	ENSP00000445210.2:n.486-22_486-20del
ENST00000566103.1:n.124-22_124-20del (WWOX)
ENST00000566780.5:c.1057-22_1057-20del (WWOX)	ENSP00000457230.1:n.1057-22_1057-20del
ENST00000569332.5:c.*854-22_*854-20del (WWOX)	ENSP00000454788.1:n.*854-22_*854-20del
NM_001291997.1:c.718-22_718-20del (WWOX)	NP_001278926.1:n.718-22_718-20del
NM_016373.3:c.1057-22_1057-20del (WWOX)	NP_057457.1:n.1057-22_1057-20del
XM_011523100.1:c.1153-22_1153-20del (WWOX)	XP_011521402.1:n.1153-22_1153-20del
XM_011523103.1:c.*29-22_*29-20del (WWOX)	XP_011521405.1:n.*29-22_*29-20del
XR_933762.1:n.13_15del
XM_011523103.3:c.*29-22_*29-20del (WWOX)	XP_011521405.1:n.*29-22_*29-20del
XM_017023279.1:c.143-22_143-20del (WWOX)	XP_016878768.1:n.143-22_143-20del
XM_024450279.1:c.*1342_*1344del (MAF)	XP_024306047.1:n.*1342_*1344del
XR_001751902.2:n.4544_4546del (MAF)
XR_002957802.1:n.4544_4546del (MAF)
XR_002957803.1:n.4544_4546del (MAF)
XR_002957804.1:n.4544_4546del (MAF)
NM_016373.4:c.1057-22_1057-20del (WWOX) MANE Select	NP_057457.1:n.1057-22_1057-20del
NM_001291997.2:c.718-22_718-20del (WWOX)	NP_001278926.1:n.718-22_718-20del