Canonical Allele Identifier: CA2672776406

Gene: WWC2

Linked Data

• gnomAD v4: 4-183289767-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289772del , CM000666.2:g.183289772del	GRCh38
NC_000004.11:g.184210925del , CM000666.1:g.184210925del	GRCh37
NC_000004.10:g.184447919del	NCBI36
NG_051586.1:g.196138del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3384+137del MANE Select	ENSP00000384222.3:n.3384+137del
ENST00000403733.7:c.3384+137del	ENSP00000384222.3:n.3384+137del
ENST00000427431.5:c.*2776+137del	ENSP00000393342.1:n.*2776+137del
ENST00000438543.5:c.*1180+137del	ENSP00000413521.1:n.*1180+137del
ENST00000448232.6:c.3456+137del	ENSP00000398577.2:n.3456+137del
ENST00000504005.5:c.2430+137del	ENSP00000427569.1:n.2430+137del
ENST00000508747.1:c.768+137del	ENSP00000420835.1:n.768+137del
ENST00000513834.5:c.3237+137del	ENSP00000425054.1:n.3237+137del
NM_024949.5:c.3384+137del	NP_079225.5:n.3384+137del
XM_011532269.1:c.3456+137del	XP_011530571.1:n.3456+137del
XM_011532269.3:c.3456+137del	XP_011530571.1:n.3456+137del
XM_024454225.1:c.3162+137del	XP_024309993.1:n.3162+137del
NM_024949.6:c.3384+137del MANE Select	NP_079225.5:n.3384+137del