Canonical Allele Identifier: CA396843290

Gene: WWOX

Linked Data

• gnomAD v4: 16-78432619-A-C
• MyVariant Identifiers: chr16:g.78466516A>C (hg19) ; chr16:g.78432619A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78432619A>C , CM000678.2:g.78432619A>C	GRCh38
NC_000016.9:g.78466516A>C , CM000678.1:g.78466516A>C	GRCh37
NC_000016.8:g.77024017A>C	NCBI36
NG_011698.1:g.337966A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000627394.3:c.923A>C	ENSP00000485925.2:p.His308Pro
ENST00000683929.1:c.923A>C	ENSP00000507689.1:p.His308Pro
ENST00000684632.1:n.1302A>C
ENST00000566780.6:c.923A>C MANE Select	ENSP00000457230.1:p.His308Pro
ENST00000402655.6:c.409+317465A>C	ENSP00000384238.2:n.409+317465A>C
ENST00000406884.6:c.516+268330A>C	ENSP00000384495.2:n.516+268330A>C
ENST00000408984.7:c.923A>C	ENSP00000386161.3:p.His308Pro
ENST00000539474.6:c.409+317465A>C	ENSP00000445210.2:n.409+317465A>C
ENST00000566780.5:c.923A>C	ENSP00000457230.1:p.His308Pro
ENST00000569332.5:c.*720A>C	ENSP00000454788.1:n.*720A>C
ENST00000620008.1:c.317A>C	ENSP00000482648.1:p.His106Pro
NM_001291997.1:c.584A>C	NP_001278926.1:p.His195Pro
NM_016373.3:c.923A>C	NP_057457.1:p.His308Pro
XM_006721195.2:c.923A>C	XP_006721258.1:p.His308Pro
XM_011523100.1:c.923A>C	XP_011521402.1:p.His308Pro
XM_011523101.1:c.923A>C	XP_011521403.1:p.His308Pro
XM_011523102.1:c.923A>C	XP_011521404.1:p.His308Pro
XM_011523103.1:c.923A>C	XP_011521405.1:p.His308Pro
XM_011523104.1:c.923A>C	XP_011521406.1:p.His308Pro
XR_933765.1:n.3418+1701T>G
XM_011523101.3:c.923A>C	XP_011521403.1:p.His308Pro
XM_011523103.3:c.923A>C	XP_011521405.1:p.His308Pro
XM_011523104.3:c.923A>C	XP_011521406.1:p.His308Pro
NM_016373.4:c.923A>C MANE Select	NP_057457.1:p.His308Pro
NM_001291997.2:c.584A>C	NP_001278926.1:p.His195Pro