Canonical Allele Identifier: CA2707765872

Gene: WWC2

Linked Data

• dbSNP Id: rs2111074933

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289134_183289158del , CM000666.2:g.183289134_183289158del	GRCh38
NC_000004.11:g.184210287_184210311del , CM000666.1:g.184210287_184210311del	GRCh37
NC_000004.10:g.184447281_184447305del	NCBI36
NG_051586.1:g.195500_195524del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3142-259_3142-235del MANE Select	ENSP00000384222.3:n.3142-259_3142-235del
ENST00000403733.7:c.3142-259_3142-235del	ENSP00000384222.3:n.3142-259_3142-235del
ENST00000427431.5:c.*2534-259_*2534-235del	ENSP00000393342.1:n.*2534-259_*2534-235del
ENST00000438543.5:c.*938-259_*938-235del	ENSP00000413521.1:n.*938-259_*938-235del
ENST00000448232.6:c.3214-259_3214-235del	ENSP00000398577.2:n.3214-259_3214-235del
ENST00000504005.5:c.2188-259_2188-235del	ENSP00000427569.1:n.2188-259_2188-235del
ENST00000508747.1:c.526-259_526-235del	ENSP00000420835.1:n.526-259_526-235del
ENST00000513834.5:c.2995-259_2995-235del	ENSP00000425054.1:n.2995-259_2995-235del
NM_024949.5:c.3142-259_3142-235del	NP_079225.5:n.3142-259_3142-235del
XM_011532269.1:c.3214-259_3214-235del	XP_011530571.1:n.3214-259_3214-235del
XM_011532269.3:c.3214-259_3214-235del	XP_011530571.1:n.3214-259_3214-235del
XM_024454225.1:c.2920-259_2920-235del	XP_024309993.1:n.2920-259_2920-235del
NM_024949.6:c.3142-259_3142-235del MANE Select	NP_079225.5:n.3142-259_3142-235del