Canonical Allele Identifier: CA2764796793

Gene: WWC2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289747_183289748insCGTCA , CM000666.2:g.183289747_183289748insCGTCA	GRCh38
NC_000004.11:g.184210900_184210901insCGTCA , CM000666.1:g.184210900_184210901insCGTCA	GRCh37
NC_000004.10:g.184447894_184447895insCGTCA	NCBI36
NG_051586.1:g.196113_196114insCGTCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3384+112_3384+113insCGTCA MANE Select	ENSP00000384222.3:n.3384+112_3384+113insCGTCA
ENST00000403733.7:c.3384+112_3384+113insCGTCA	ENSP00000384222.3:n.3384+112_3384+113insCGTCA
ENST00000427431.5:c.*2776+112_*2776+113insCGTCA	ENSP00000393342.1:n.*2776+112_*2776+113insCGTCA
ENST00000438543.5:c.*1180+112_*1180+113insCGTCA	ENSP00000413521.1:n.*1180+112_*1180+113insCGTCA
ENST00000448232.6:c.3456+112_3456+113insCGTCA	ENSP00000398577.2:n.3456+112_3456+113insCGTCA
ENST00000504005.5:c.2430+112_2430+113insCGTCA	ENSP00000427569.1:n.2430+112_2430+113insCGTCA
ENST00000508747.1:c.768+112_768+113insCGTCA	ENSP00000420835.1:n.768+112_768+113insCGTCA
ENST00000513834.5:c.3237+112_3237+113insCGTCA	ENSP00000425054.1:n.3237+112_3237+113insCGTCA
NM_024949.5:c.3384+112_3384+113insCGTCA	NP_079225.5:n.3384+112_3384+113insCGTCA
XM_011532269.1:c.3456+112_3456+113insCGTCA	XP_011530571.1:n.3456+112_3456+113insCGTCA
XM_011532269.3:c.3456+112_3456+113insCGTCA	XP_011530571.1:n.3456+112_3456+113insCGTCA
XM_024454225.1:c.3162+112_3162+113insCGTCA	XP_024309993.1:n.3162+112_3162+113insCGTCA
NM_024949.6:c.3384+112_3384+113insCGTCA MANE Select	NP_079225.5:n.3384+112_3384+113insCGTCA