Canonical Allele Identifier: CA724396390

Gene: WWOX MAF

Linked Data

• dbSNP Id: rs1417102732
• MyVariant Identifiers: chr16:g.79238589T>G (hg19) ; chr16:g.79204692T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.79204692T>G , CM000678.2:g.79204692T>G	GRCh38
NC_000016.9:g.79238589T>G , CM000678.1:g.79238589T>G	GRCh37
NC_000016.8:g.77796090T>G	NCBI36
NG_011698.1:g.1110039T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000683929.1:c.*171-6916T>G (WWOX)	ENSP00000507689.1:n.*171-6916T>G
ENST00000566780.6:c.1057-6916T>G (WWOX) MANE Select	ENSP00000457230.1:n.1057-6916T>G
ENST00000402655.6:c.410-6916T>G (WWOX)	ENSP00000384238.2:n.410-6916T>G
ENST00000406884.6:c.517-6916T>G (WWOX)	ENSP00000384495.2:n.517-6916T>G
ENST00000539474.6:c.486-6916T>G (WWOX)	ENSP00000445210.2:n.486-6916T>G
ENST00000566103.1:n.124-6916T>G (WWOX)
ENST00000566780.5:c.1057-6916T>G (WWOX)	ENSP00000457230.1:n.1057-6916T>G
ENST00000569332.5:c.*854-6916T>G (WWOX)	ENSP00000454788.1:n.*854-6916T>G
NM_001291997.1:c.718-6916T>G (WWOX)	NP_001278926.1:n.718-6916T>G
NM_016373.3:c.1057-6916T>G (WWOX)	NP_057457.1:n.1057-6916T>G
XM_011523100.1:c.1153-6916T>G (WWOX)	XP_011521402.1:n.1153-6916T>G
XM_011523103.1:c.*29-6916T>G (WWOX)	XP_011521405.1:n.*29-6916T>G
XR_933762.1:n.6361A>C
XM_011523103.3:c.*29-6916T>G (WWOX)	XP_011521405.1:n.*29-6916T>G
XM_017023279.1:c.143-6916T>G (WWOX)	XP_016878768.1:n.143-6916T>G
XM_024450279.1:c.*8238A>C (MAF)	XP_024306047.1:n.*8238A>C
XR_001751902.2:n.9889A>C (MAF)
XR_002957802.1:n.10506A>C (MAF)
XR_002957803.1:n.10892A>C (MAF)
XR_002957804.1:n.9817A>C (MAF)
NM_016373.4:c.1057-6916T>G (WWOX) MANE Select	NP_057457.1:n.1057-6916T>G
NM_001291997.2:c.718-6916T>G (WWOX)	NP_001278926.1:n.718-6916T>G