Canonical Allele Identifier: CA2634409677

Gene: WWOX

Linked Data

• gnomAD v4: 16-78099463-T-TCCA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78099463_78099464insCCA , CM000678.2:g.78099463_78099464insCCA	GRCh38
NC_000016.9:g.78133360_78133361insCCA , CM000678.1:g.78133360_78133361insCCA	GRCh37
NC_000016.8:g.76690861_76690862insCCA	NCBI36
NG_011698.1:g.4810_4811insCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627394.3:c.-316_-315insCCA	ENSP00000485925.2:n.-316_-315insCCA
ENST00000682609.1:n.12_13insCCA
ENST00000683286.1:n.12_13insCCA
ENST00000683929.1:c.-316_-315insCCA	ENSP00000507689.1:n.-316_-315insCCA
ENST00000684070.1:n.14_15insCCA
ENST00000684381.1:n.12_13insCCA
ENST00000684452.1:n.12_13insCCA
ENST00000684632.1:n.64_65insCCA
ENST00000566780.5:c.-316_-315insCCA	ENSP00000457230.1:n.-316_-315insCCA
ENST00000627394.2:c.-316_-315insCCA	ENSP00000485925.1:n.-316_-315insCCA
NM_001291997.1:c.-590_-589insCCA	NP_001278926.1:n.-590_-589insCCA
NM_016373.3:c.-316_-315insCCA	NP_057457.1:n.-316_-315insCCA
NM_130791.3:c.-316_-315insCCA	NP_570607.1:n.-316_-315insCCA
NR_120435.1:n.51_52insCCA
NR_120436.1:n.51_52insCCA