Canonical Allele Identifier: CA623626138

Gene: WWOX

Linked Data

• ClinVar Variation Id: 450592
• ClinVar RCV Id: RCV000522383 ; RCV000850619 ; RCV000703936 ; RCV003152608
• dbSNP Id: rs1039151413
• gnomAD v2: 16-78420850-G-A
• gnomAD v4: 16-78386953-G-A
• MyVariant Identifiers: chr16:g.78420850G>A (hg19) ; chr16:g.78386953G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78386953G>A , CM000678.2:g.78386953G>A	GRCh38
NC_000016.9:g.78420850G>A , CM000678.1:g.78420850G>A	GRCh37
NC_000016.8:g.76978351G>A	NCBI36
NG_011698.1:g.292300G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627394.3:c.605+5G>A	ENSP00000485925.2:n.605+5G>A
ENST00000683929.1:c.605+5G>A	ENSP00000507689.1:n.605+5G>A
ENST00000684070.1:n.874G>A
ENST00000684632.1:n.984+5G>A
ENST00000566780.6:c.605+5G>A MANE Select	ENSP00000457230.1:n.605+5G>A
ENST00000402655.6:c.409+271799G>A	ENSP00000384238.2:n.409+271799G>A
ENST00000406884.6:c.516+222664G>A	ENSP00000384495.2:n.516+222664G>A
ENST00000408984.7:c.605+5G>A	ENSP00000386161.3:n.605+5G>A
ENST00000539474.6:c.409+271799G>A	ENSP00000445210.2:n.409+271799G>A
ENST00000562639.5:n.293+5G>A
ENST00000566662.5:c.*223+5G>A	ENSP00000454331.1:n.*223+5G>A
ENST00000566780.5:c.605+5G>A	ENSP00000457230.1:n.605+5G>A
ENST00000569332.5:c.*402+5G>A	ENSP00000454788.1:n.*402+5G>A
NM_001291997.1:c.266+5G>A	NP_001278926.1:n.266+5G>A
NM_016373.3:c.605+5G>A	NP_057457.1:n.605+5G>A
XM_006721195.2:c.605+5G>A	XP_006721258.1:n.605+5G>A
XM_011523100.1:c.605+5G>A	XP_011521402.1:n.605+5G>A
XM_011523101.1:c.605+5G>A	XP_011521403.1:n.605+5G>A
XM_011523102.1:c.605+5G>A	XP_011521404.1:n.605+5G>A
XM_011523103.1:c.605+5G>A	XP_011521405.1:n.605+5G>A
XM_011523104.1:c.605+5G>A	XP_011521406.1:n.605+5G>A
XM_011523101.3:c.605+5G>A	XP_011521403.1:n.605+5G>A
XM_011523103.3:c.605+5G>A	XP_011521405.1:n.605+5G>A
XM_011523104.3:c.605+5G>A	XP_011521406.1:n.605+5G>A
NM_016373.4:c.605+5G>A MANE Select	NP_057457.1:n.605+5G>A
NM_001291997.2:c.266+5G>A	NP_001278926.1:n.266+5G>A