Canonical Allele Identifier: CA2764796795

Gene: WWC2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289753_183289754insTC , CM000666.2:g.183289753_183289754insTC	GRCh38
NC_000004.11:g.184210906_184210907insTC , CM000666.1:g.184210906_184210907insTC	GRCh37
NC_000004.10:g.184447900_184447901insTC	NCBI36
NG_051586.1:g.196119_196120insTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3384+118_3384+119insTC MANE Select	ENSP00000384222.3:n.3384+118_3384+119insTC
ENST00000403733.7:c.3384+118_3384+119insTC	ENSP00000384222.3:n.3384+118_3384+119insTC
ENST00000427431.5:c.*2776+118_*2776+119insTC	ENSP00000393342.1:n.*2776+118_*2776+119insTC
ENST00000438543.5:c.*1180+118_*1180+119insTC	ENSP00000413521.1:n.*1180+118_*1180+119insTC
ENST00000448232.6:c.3456+118_3456+119insTC	ENSP00000398577.2:n.3456+118_3456+119insTC
ENST00000504005.5:c.2430+118_2430+119insTC	ENSP00000427569.1:n.2430+118_2430+119insTC
ENST00000508747.1:c.768+118_768+119insTC	ENSP00000420835.1:n.768+118_768+119insTC
ENST00000513834.5:c.3237+118_3237+119insTC	ENSP00000425054.1:n.3237+118_3237+119insTC
NM_024949.5:c.3384+118_3384+119insTC	NP_079225.5:n.3384+118_3384+119insTC
XM_011532269.1:c.3456+118_3456+119insTC	XP_011530571.1:n.3456+118_3456+119insTC
XM_011532269.3:c.3456+118_3456+119insTC	XP_011530571.1:n.3456+118_3456+119insTC
XM_024454225.1:c.3162+118_3162+119insTC	XP_024309993.1:n.3162+118_3162+119insTC
NM_024949.6:c.3384+118_3384+119insTC MANE Select	NP_079225.5:n.3384+118_3384+119insTC