Canonical Allele Identifier: CA2764796794

Gene: WWC2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289749_183289750insCCGTTTCTA , CM000666.2:g.183289749_183289750insCCGTTTCTA	GRCh38
NC_000004.11:g.184210902_184210903insCCGTTTCTA , CM000666.1:g.184210902_184210903insCCGTTTCTA	GRCh37
NC_000004.10:g.184447896_184447897insCCGTTTCTA	NCBI36
NG_051586.1:g.196115_196116insCCGTTTCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3384+114_3384+115insCCGTTTCTA MANE Select	ENSP00000384222.3:n.3384+114_3384+115insCCGTTTCTA
ENST00000403733.7:c.3384+114_3384+115insCCGTTTCTA	ENSP00000384222.3:n.3384+114_3384+115insCCGTTTCTA
ENST00000427431.5:c.*2776+114_*2776+115insCCGTTTCTA	ENSP00000393342.1:n.*2776+114_*2776+115insCCGTTTCTA
ENST00000438543.5:c.*1180+114_*1180+115insCCGTTTCTA	ENSP00000413521.1:n.*1180+114_*1180+115insCCGTTTCTA
ENST00000448232.6:c.3456+114_3456+115insCCGTTTCTA	ENSP00000398577.2:n.3456+114_3456+115insCCGTTTCTA
ENST00000504005.5:c.2430+114_2430+115insCCGTTTCTA	ENSP00000427569.1:n.2430+114_2430+115insCCGTTTCTA
ENST00000508747.1:c.768+114_768+115insCCGTTTCTA	ENSP00000420835.1:n.768+114_768+115insCCGTTTCTA
ENST00000513834.5:c.3237+114_3237+115insCCGTTTCTA	ENSP00000425054.1:n.3237+114_3237+115insCCGTTTCTA
NM_024949.5:c.3384+114_3384+115insCCGTTTCTA	NP_079225.5:n.3384+114_3384+115insCCGTTTCTA
XM_011532269.1:c.3456+114_3456+115insCCGTTTCTA	XP_011530571.1:n.3456+114_3456+115insCCGTTTCTA
XM_011532269.3:c.3456+114_3456+115insCCGTTTCTA	XP_011530571.1:n.3456+114_3456+115insCCGTTTCTA
XM_024454225.1:c.3162+114_3162+115insCCGTTTCTA	XP_024309993.1:n.3162+114_3162+115insCCGTTTCTA
NM_024949.6:c.3384+114_3384+115insCCGTTTCTA MANE Select	NP_079225.5:n.3384+114_3384+115insCCGTTTCTA