Canonical Allele Identifier: CA623600919

Gene: WWOX

Linked Data

• dbSNP Id: rs1310588198
• gnomAD v2: 16-78133311-T-TC
• gnomAD v3: 16-78099414-T-TC
• gnomAD v4: 16-78099414-T-TC
• MyVariant Identifiers: chr16:g.78133311_78133312insC (hg19) ; chr16:g.78099414_78099415insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78099416dup , CM000678.2:g.78099416dup	GRCh38
NC_000016.9:g.78133313dup , CM000678.1:g.78133313dup	GRCh37
NC_000016.8:g.76690814dup	NCBI36
NG_011698.1:g.4763dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627394.3:c.-363dup	ENSP00000485925.2:n.-363dup
ENST00000683929.1:c.-363dup	ENSP00000507689.1:n.-363dup
ENST00000684632.1:n.17dup
ENST00000566780.5:c.-363dup	ENSP00000457230.1:n.-363dup
NM_001291997.1:c.-637dup	NP_001278926.1:n.-637dup
NM_016373.3:c.-363dup	NP_057457.1:n.-363dup
NM_130791.3:c.-363dup	NP_570607.1:n.-363dup
NR_120435.1:n.4dup
NR_120436.1:n.4dup