Canonical Allele Identifier: CA284501994

Gene: WWOX

Linked Data

• dbSNP Id: rs955985790
• MyVariant Identifiers: chr16:g.78133543del (hg19) ; chr16:g.78099646del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78099646del , CM000678.2:g.78099646del	GRCh38
NC_000016.9:g.78133543del , CM000678.1:g.78133543del	GRCh37
NC_000016.8:g.76691044del	NCBI36
NG_011698.1:g.4993del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627394.3:c.-133del	ENSP00000485925.2:n.-133del
ENST00000682609.1:n.195del
ENST00000683286.1:n.195del
ENST00000683929.1:c.-133del	ENSP00000507689.1:n.-133del
ENST00000684070.1:n.197del
ENST00000684381.1:n.195del
ENST00000684452.1:n.195del
ENST00000684632.1:n.247del
ENST00000566780.5:c.-133del	ENSP00000457230.1:n.-133del
ENST00000569332.5:c.-133del	ENSP00000454788.1:n.-133del
ENST00000627394.2:c.-133del	ENSP00000485925.1:n.-133del
NM_001291997.1:c.-407del	NP_001278926.1:n.-407del
NM_016373.3:c.-133del	NP_057457.1:n.-133del
NM_130791.3:c.-133del	NP_570607.1:n.-133del
NR_120435.1:n.234del
NR_120436.1:n.234del