Canonical Allele Identifier: CA396536991

Gene: WWOX MAF

Linked Data

• ClinVar Variation Id: 1047640
• ClinVar RCV Id: RCV001352381
• dbSNP Id: rs2051754918
• MyVariant Identifiers: chr16:g.79245532T>C (hg19) ; chr16:g.79211635T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.79211635T>C , CM000678.2:g.79211635T>C	GRCh38
NC_000016.9:g.79245532T>C , CM000678.1:g.79245532T>C	GRCh37
NC_000016.8:g.77803033T>C	NCBI36
NG_011698.1:g.1116982T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683929.1:c.*198T>C (WWOX)	ENSP00000507689.1:n.*198T>C
ENST00000566780.6:c.1084T>C (WWOX) MANE Select	ENSP00000457230.1:p.Cys362Arg
ENST00000402655.6:c.437T>C (WWOX)	ENSP00000384238.2:p.Leu146Pro
ENST00000406884.6:c.544T>C (WWOX)	ENSP00000384495.2:p.Cys182Arg
ENST00000539474.6:c.513T>C (WWOX)	ENSP00000445210.2:p.Thr171=
ENST00000566103.1:n.151T>C (WWOX)
ENST00000566780.5:c.1084T>C (WWOX)	ENSP00000457230.1:p.Cys362Arg
ENST00000569332.5:c.*881T>C (WWOX)	ENSP00000454788.1:n.*881T>C
NM_001291997.1:c.745T>C (WWOX)	NP_001278926.1:p.Cys249Arg
NM_016373.3:c.1084T>C (WWOX)	NP_057457.1:p.Cys362Arg
XM_011523100.1:c.1180T>C (WWOX)	XP_011521402.1:p.Cys394Arg
XM_011523103.1:c.*56T>C (WWOX)	XP_011521405.1:n.*56T>C
XM_011523103.3:c.*56T>C (WWOX)	XP_011521405.1:n.*56T>C
XM_017023279.1:c.170T>C (WWOX)	XP_016878768.1:p.Leu57Pro
XM_024450279.1:c.*1295A>G (MAF)	XP_024306047.1:n.*1295A>G
XR_001751902.2:n.4497A>G (MAF)
XR_002957802.1:n.4497A>G (MAF)
XR_002957803.1:n.4497A>G (MAF)
XR_002957804.1:n.4497A>G (MAF)
NM_016373.4:c.1084T>C (WWOX) MANE Select	NP_057457.1:p.Cys362Arg
NM_001291997.2:c.745T>C (WWOX)	NP_001278926.1:p.Cys249Arg