Canonical Allele Identifier: CA396843095

Gene: WWOX

Linked Data

• gnomAD v4: 16-78432520-T-G
• MyVariant Identifiers: chr16:g.78466417T>G (hg19) ; chr16:g.78432520T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78432520T>G , CM000678.2:g.78432520T>G	GRCh38
NC_000016.9:g.78466417T>G , CM000678.1:g.78466417T>G	GRCh37
NC_000016.8:g.77023918T>G	NCBI36
NG_011698.1:g.337867T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000627394.3:c.824T>G	ENSP00000485925.2:p.Leu275Arg
ENST00000683929.1:c.824T>G	ENSP00000507689.1:p.Leu275Arg
ENST00000684632.1:n.1203T>G
ENST00000566780.6:c.824T>G MANE Select	ENSP00000457230.1:p.Leu275Arg
ENST00000402655.6:c.409+317366T>G	ENSP00000384238.2:n.409+317366T>G
ENST00000406884.6:c.516+268231T>G	ENSP00000384495.2:n.516+268231T>G
ENST00000408984.7:c.824T>G	ENSP00000386161.3:p.Leu275Arg
ENST00000539474.6:c.409+317366T>G	ENSP00000445210.2:n.409+317366T>G
ENST00000562639.5:n.512T>G
ENST00000566780.5:c.824T>G	ENSP00000457230.1:p.Leu275Arg
ENST00000569332.5:c.*621T>G	ENSP00000454788.1:n.*621T>G
ENST00000620008.1:c.218T>G	ENSP00000482648.1:p.Leu73Arg
NM_001291997.1:c.485T>G	NP_001278926.1:p.Leu162Arg
NM_016373.3:c.824T>G	NP_057457.1:p.Leu275Arg
XM_006721195.2:c.824T>G	XP_006721258.1:p.Leu275Arg
XM_011523100.1:c.824T>G	XP_011521402.1:p.Leu275Arg
XM_011523101.1:c.824T>G	XP_011521403.1:p.Leu275Arg
XM_011523102.1:c.824T>G	XP_011521404.1:p.Leu275Arg
XM_011523103.1:c.824T>G	XP_011521405.1:p.Leu275Arg
XM_011523104.1:c.824T>G	XP_011521406.1:p.Leu275Arg
XR_933765.1:n.3419-1707A>C
XM_011523101.3:c.824T>G	XP_011521403.1:p.Leu275Arg
XM_011523103.3:c.824T>G	XP_011521405.1:p.Leu275Arg
XM_011523104.3:c.824T>G	XP_011521406.1:p.Leu275Arg
NM_016373.4:c.824T>G MANE Select	NP_057457.1:p.Leu275Arg
NM_001291997.2:c.485T>G	NP_001278926.1:p.Leu162Arg