Canonical Allele Identifier: CA2764796801

Gene: WWC2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289815_183289816insCAG , CM000666.2:g.183289815_183289816insCAG	GRCh38
NC_000004.11:g.184210968_184210969insCAG , CM000666.1:g.184210968_184210969insCAG	GRCh37
NC_000004.10:g.184447962_184447963insCAG	NCBI36
NG_051586.1:g.196181_196182insCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3384+180_3384+181insCAG MANE Select	ENSP00000384222.3:n.3384+180_3384+181insCAG
ENST00000403733.7:c.3384+180_3384+181insCAG	ENSP00000384222.3:n.3384+180_3384+181insCAG
ENST00000427431.5:c.*2776+180_*2776+181insCAG	ENSP00000393342.1:n.*2776+180_*2776+181insCAG
ENST00000438543.5:c.*1180+180_*1180+181insCAG	ENSP00000413521.1:n.*1180+180_*1180+181insCAG
ENST00000448232.6:c.3456+180_3456+181insCAG	ENSP00000398577.2:n.3456+180_3456+181insCAG
ENST00000504005.5:c.2430+180_2430+181insCAG	ENSP00000427569.1:n.2430+180_2430+181insCAG
ENST00000508747.1:c.768+180_768+181insCAG	ENSP00000420835.1:n.768+180_768+181insCAG
ENST00000513834.5:c.3237+180_3237+181insCAG	ENSP00000425054.1:n.3237+180_3237+181insCAG
NM_024949.5:c.3384+180_3384+181insCAG	NP_079225.5:n.3384+180_3384+181insCAG
XM_011532269.1:c.3456+180_3456+181insCAG	XP_011530571.1:n.3456+180_3456+181insCAG
XM_011532269.3:c.3456+180_3456+181insCAG	XP_011530571.1:n.3456+180_3456+181insCAG
XM_024454225.1:c.3162+180_3162+181insCAG	XP_024309993.1:n.3162+180_3162+181insCAG
NM_024949.6:c.3384+180_3384+181insCAG MANE Select	NP_079225.5:n.3384+180_3384+181insCAG