Canonical Allele Identifier: CA2672776358

Gene: WWC2

Linked Data

• gnomAD v4: 4-183289703-GTACCCAAC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289705_183289712del , CM000666.2:g.183289705_183289712del	GRCh38
NC_000004.11:g.184210858_184210865del , CM000666.1:g.184210858_184210865del	GRCh37
NC_000004.10:g.184447852_184447859del	NCBI36
NG_051586.1:g.196071_196078del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3384+70_3384+77del MANE Select	ENSP00000384222.3:n.3384+70_3384+77del
ENST00000403733.7:c.3384+70_3384+77del	ENSP00000384222.3:n.3384+70_3384+77del
ENST00000427431.5:c.*2776+70_*2776+77del	ENSP00000393342.1:n.*2776+70_*2776+77del
ENST00000438543.5:c.*1180+70_*1180+77del	ENSP00000413521.1:n.*1180+70_*1180+77del
ENST00000448232.6:c.3456+70_3456+77del	ENSP00000398577.2:n.3456+70_3456+77del
ENST00000504005.5:c.2430+70_2430+77del	ENSP00000427569.1:n.2430+70_2430+77del
ENST00000508747.1:c.768+70_768+77del	ENSP00000420835.1:n.768+70_768+77del
ENST00000513834.5:c.3237+70_3237+77del	ENSP00000425054.1:n.3237+70_3237+77del
NM_024949.5:c.3384+70_3384+77del	NP_079225.5:n.3384+70_3384+77del
XM_011532269.1:c.3456+70_3456+77del	XP_011530571.1:n.3456+70_3456+77del
XM_011532269.3:c.3456+70_3456+77del	XP_011530571.1:n.3456+70_3456+77del
XM_024454225.1:c.3162+70_3162+77del	XP_024309993.1:n.3162+70_3162+77del
NM_024949.6:c.3384+70_3384+77del MANE Select	NP_079225.5:n.3384+70_3384+77del