Canonical Allele Identifier: CA2764796787

Gene: WWC2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289419_183289420insC , CM000666.2:g.183289419_183289420insC	GRCh38
NC_000004.11:g.184210572_184210573insC , CM000666.1:g.184210572_184210573insC	GRCh37
NC_000004.10:g.184447566_184447567insC	NCBI36
NG_051586.1:g.195785_195786insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3168_3169insC MANE Select	ENSP00000384222.3:p.Thr1057HisfsTer29
ENST00000403733.7:c.3168_3169insC	ENSP00000384222.3:p.Thr1057HisfsTer29
ENST00000427431.5:c.*2560_*2561insC	ENSP00000393342.1:n.*2560_*2561insC
ENST00000438543.5:c.*964_*965insC	ENSP00000413521.1:n.*964_*965insC
ENST00000448232.6:c.3240_3241insC	ENSP00000398577.2:p.Thr1081HisfsTer29
ENST00000504005.5:c.2214_2215insC	ENSP00000427569.1:p.Thr739HisfsTer29
ENST00000508747.1:c.552_553insC	ENSP00000420835.1:p.Thr185HisfsTer29
ENST00000513834.5:c.3021_3022insC	ENSP00000425054.1:p.Thr1008HisfsTer29
NM_024949.5:c.3168_3169insC	NP_079225.5:p.Thr1057HisfsTer29
XM_011532269.1:c.3240_3241insC	XP_011530571.1:p.Thr1081HisfsTer29
XM_011532269.3:c.3240_3241insC	XP_011530571.1:p.Thr1081HisfsTer29
XM_024454225.1:c.2946_2947insC	XP_024309993.1:p.Thr983HisfsTer29
NM_024949.6:c.3168_3169insC MANE Select	NP_079225.5:p.Thr1057HisfsTer29