Canonical Allele Identifier: CA1518546802

Gene: WWC2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289676_183289677delinsCT , CM000666.2:g.183289676_183289677delinsCT	GRCh38
NC_000004.11:g.184210829_184210830delinsCT , CM000666.1:g.184210829_184210830delinsCT	GRCh37
NC_000004.10:g.184447823_184447824delinsCT	NCBI36
NG_051586.1:g.196042_196043delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3384+41_3384+42delinsCT MANE Select	ENSP00000384222.3:n.3384+41_3384+42delinsCT
ENST00000403733.7:c.3384+41_3384+42delinsCT	ENSP00000384222.3:n.3384+41_3384+42delinsCT
ENST00000427431.5:c.*2776+41_*2776+42delinsCT	ENSP00000393342.1:n.*2776+41_*2776+42delinsCT
ENST00000438543.5:c.*1180+41_*1180+42delinsCT	ENSP00000413521.1:n.*1180+41_*1180+42delinsCT
ENST00000448232.6:c.3456+41_3456+42delinsCT	ENSP00000398577.2:n.3456+41_3456+42delinsCT
ENST00000504005.5:c.2430+41_2430+42delinsCT	ENSP00000427569.1:n.2430+41_2430+42delinsCT
ENST00000508747.1:c.768+41_768+42delinsCT	ENSP00000420835.1:n.768+41_768+42delinsCT
ENST00000513834.5:c.3237+41_3237+42delinsCT	ENSP00000425054.1:n.3237+41_3237+42delinsCT
NM_024949.5:c.3384+41_3384+42delinsCT	NP_079225.5:n.3384+41_3384+42delinsCT
XM_011532269.1:c.3456+41_3456+42delinsCT	XP_011530571.1:n.3456+41_3456+42delinsCT
XM_011532269.3:c.3456+41_3456+42delinsCT	XP_011530571.1:n.3456+41_3456+42delinsCT
XM_024454225.1:c.3162+41_3162+42delinsCT	XP_024309993.1:n.3162+41_3162+42delinsCT
NM_024949.6:c.3384+41_3384+42delinsCT MANE Select	NP_079225.5:n.3384+41_3384+42delinsCT