Canonical Allele Identifier: CA1518546834

Gene: WWC2

Linked Data

• dbSNP Id: rs1738378077
• gnomAD v4: 4-183289732-TAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289733_183289734del , CM000666.2:g.183289733_183289734del	GRCh38
NC_000004.11:g.184210886_184210887del , CM000666.1:g.184210886_184210887del	GRCh37
NC_000004.10:g.184447880_184447881del	NCBI36
NG_051586.1:g.196099_196100del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3384+98_3384+99del MANE Select	ENSP00000384222.3:n.3384+98_3384+99del
ENST00000403733.7:c.3384+98_3384+99del	ENSP00000384222.3:n.3384+98_3384+99del
ENST00000427431.5:c.*2776+98_*2776+99del	ENSP00000393342.1:n.*2776+98_*2776+99del
ENST00000438543.5:c.*1180+98_*1180+99del	ENSP00000413521.1:n.*1180+98_*1180+99del
ENST00000448232.6:c.3456+98_3456+99del	ENSP00000398577.2:n.3456+98_3456+99del
ENST00000504005.5:c.2430+98_2430+99del	ENSP00000427569.1:n.2430+98_2430+99del
ENST00000508747.1:c.768+98_768+99del	ENSP00000420835.1:n.768+98_768+99del
ENST00000513834.5:c.3237+98_3237+99del	ENSP00000425054.1:n.3237+98_3237+99del
NM_024949.5:c.3384+98_3384+99del	NP_079225.5:n.3384+98_3384+99del
XM_011532269.1:c.3456+98_3456+99del	XP_011530571.1:n.3456+98_3456+99del
XM_011532269.3:c.3456+98_3456+99del	XP_011530571.1:n.3456+98_3456+99del
XM_024454225.1:c.3162+98_3162+99del	XP_024309993.1:n.3162+98_3162+99del
NM_024949.6:c.3384+98_3384+99del MANE Select	NP_079225.5:n.3384+98_3384+99del