Canonical Allele Identifier: CA1518546848

Gene: WWC2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289764_183289766delinsCAT , CM000666.2:g.183289764_183289766delinsCAT	GRCh38
NC_000004.11:g.184210917_184210919delinsCAT , CM000666.1:g.184210917_184210919delinsCAT	GRCh37
NC_000004.10:g.184447911_184447913delinsCAT	NCBI36
NG_051586.1:g.196130_196132delinsCAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3384+129_3384+131delinsCAT MANE Select	ENSP00000384222.3:n.3384+129_3384+131delinsCAT
ENST00000403733.7:c.3384+129_3384+131delinsCAT	ENSP00000384222.3:n.3384+129_3384+131delinsCAT
ENST00000427431.5:c.*2776+129_*2776+131delinsCAT	ENSP00000393342.1:n.*2776+129_*2776+131delinsCAT
ENST00000438543.5:c.*1180+129_*1180+131delinsCAT	ENSP00000413521.1:n.*1180+129_*1180+131delinsCAT
ENST00000448232.6:c.3456+129_3456+131delinsCAT	ENSP00000398577.2:n.3456+129_3456+131delinsCAT
ENST00000504005.5:c.2430+129_2430+131delinsCAT	ENSP00000427569.1:n.2430+129_2430+131delinsCAT
ENST00000508747.1:c.768+129_768+131delinsCAT	ENSP00000420835.1:n.768+129_768+131delinsCAT
ENST00000513834.5:c.3237+129_3237+131delinsCAT	ENSP00000425054.1:n.3237+129_3237+131delinsCAT
NM_024949.5:c.3384+129_3384+131delinsCAT	NP_079225.5:n.3384+129_3384+131delinsCAT
XM_011532269.1:c.3456+129_3456+131delinsCAT	XP_011530571.1:n.3456+129_3456+131delinsCAT
XM_011532269.3:c.3456+129_3456+131delinsCAT	XP_011530571.1:n.3456+129_3456+131delinsCAT
XM_024454225.1:c.3162+129_3162+131delinsCAT	XP_024309993.1:n.3162+129_3162+131delinsCAT
NM_024949.6:c.3384+129_3384+131delinsCAT MANE Select	NP_079225.5:n.3384+129_3384+131delinsCAT