Canonical Allele Identifier: CA396537214

Gene: WWOX MAF

Linked Data

• MyVariant Identifiers: chr16:g.79245623A>C (hg19) ; chr16:g.79211726A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.79211726A>C , CM000678.2:g.79211726A>C	GRCh38
NC_000016.9:g.79245623A>C , CM000678.1:g.79245623A>C	GRCh37
NC_000016.8:g.77803124A>C	NCBI36
NG_011698.1:g.1117073A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683929.1:c.*289A>C (WWOX)	ENSP00000507689.1:n.*289A>C
ENST00000566780.6:c.1175A>C (WWOX) MANE Select	ENSP00000457230.1:p.Glu392Ala
ENST00000402655.6:c.528A>C (WWOX)	ENSP00000384238.2:p.Arg176Ser
ENST00000406884.6:c.635A>C (WWOX)	ENSP00000384495.2:p.Glu212Ala
ENST00000539474.6:c.604A>C (WWOX)	ENSP00000445210.2:p.Arg202=
ENST00000566103.1:n.242A>C (WWOX)
ENST00000566780.5:c.1175A>C (WWOX)	ENSP00000457230.1:p.Glu392Ala
ENST00000569332.5:c.*972A>C (WWOX)	ENSP00000454788.1:n.*972A>C
NM_001291997.1:c.836A>C (WWOX)	NP_001278926.1:p.Glu279Ala
NM_016373.3:c.1175A>C (WWOX)	NP_057457.1:p.Glu392Ala
XM_011523100.1:c.1271A>C (WWOX)	XP_011521402.1:p.Glu424Ala
XM_011523103.3:c.*147A>C (WWOX)	XP_011521405.1:n.*147A>C
XM_017023279.1:c.261A>C (WWOX)	XP_016878768.1:p.Arg87Ser
XM_024450279.1:c.*1204T>G (MAF)	XP_024306047.1:n.*1204T>G
XR_001751902.2:n.4406T>G (MAF)
XR_002957802.1:n.4406T>G (MAF)
XR_002957803.1:n.4406T>G (MAF)
XR_002957804.1:n.4406T>G (MAF)
NM_016373.4:c.1175A>C (WWOX) MANE Select	NP_057457.1:p.Glu392Ala
NM_001291997.2:c.836A>C (WWOX)	NP_001278926.1:p.Glu279Ala