Canonical Allele Identifier: CA1518546791

Gene: WWC2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289661_183289662delinsCG , CM000666.2:g.183289661_183289662delinsCG	GRCh38
NC_000004.11:g.184210814_184210815delinsCG , CM000666.1:g.184210814_184210815delinsCG	GRCh37
NC_000004.10:g.184447808_184447809delinsCG	NCBI36
NG_051586.1:g.196027_196028delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3384+26_3384+27delinsCG MANE Select	ENSP00000384222.3:n.3384+26_3384+27delinsCG
ENST00000403733.7:c.3384+26_3384+27delinsCG	ENSP00000384222.3:n.3384+26_3384+27delinsCG
ENST00000427431.5:c.*2776+26_*2776+27delinsCG	ENSP00000393342.1:n.*2776+26_*2776+27delinsCG
ENST00000438543.5:c.*1180+26_*1180+27delinsCG	ENSP00000413521.1:n.*1180+26_*1180+27delinsCG
ENST00000448232.6:c.3456+26_3456+27delinsCG	ENSP00000398577.2:n.3456+26_3456+27delinsCG
ENST00000504005.5:c.2430+26_2430+27delinsCG	ENSP00000427569.1:n.2430+26_2430+27delinsCG
ENST00000508747.1:c.768+26_768+27delinsCG	ENSP00000420835.1:n.768+26_768+27delinsCG
ENST00000513834.5:c.3237+26_3237+27delinsCG	ENSP00000425054.1:n.3237+26_3237+27delinsCG
NM_024949.5:c.3384+26_3384+27delinsCG	NP_079225.5:n.3384+26_3384+27delinsCG
XM_011532269.1:c.3456+26_3456+27delinsCG	XP_011530571.1:n.3456+26_3456+27delinsCG
XM_011532269.3:c.3456+26_3456+27delinsCG	XP_011530571.1:n.3456+26_3456+27delinsCG
XM_024454225.1:c.3162+26_3162+27delinsCG	XP_024309993.1:n.3162+26_3162+27delinsCG
NM_024949.6:c.3384+26_3384+27delinsCG MANE Select	NP_079225.5:n.3384+26_3384+27delinsCG