Canonical Allele Identifier: CA2672776386

Gene: WWC2

Linked Data

• gnomAD v4: 4-183289737-CTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289739_183289740del , CM000666.2:g.183289739_183289740del	GRCh38
NC_000004.11:g.184210892_184210893del , CM000666.1:g.184210892_184210893del	GRCh37
NC_000004.10:g.184447886_184447887del	NCBI36
NG_051586.1:g.196105_196106del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3384+104_3384+105del MANE Select	ENSP00000384222.3:n.3384+104_3384+105del
ENST00000403733.7:c.3384+104_3384+105del	ENSP00000384222.3:n.3384+104_3384+105del
ENST00000427431.5:c.*2776+104_*2776+105del	ENSP00000393342.1:n.*2776+104_*2776+105del
ENST00000438543.5:c.*1180+104_*1180+105del	ENSP00000413521.1:n.*1180+104_*1180+105del
ENST00000448232.6:c.3456+104_3456+105del	ENSP00000398577.2:n.3456+104_3456+105del
ENST00000504005.5:c.2430+104_2430+105del	ENSP00000427569.1:n.2430+104_2430+105del
ENST00000508747.1:c.768+104_768+105del	ENSP00000420835.1:n.768+104_768+105del
ENST00000513834.5:c.3237+104_3237+105del	ENSP00000425054.1:n.3237+104_3237+105del
NM_024949.5:c.3384+104_3384+105del	NP_079225.5:n.3384+104_3384+105del
XM_011532269.1:c.3456+104_3456+105del	XP_011530571.1:n.3456+104_3456+105del
XM_011532269.3:c.3456+104_3456+105del	XP_011530571.1:n.3456+104_3456+105del
XM_024454225.1:c.3162+104_3162+105del	XP_024309993.1:n.3162+104_3162+105del
NM_024949.6:c.3384+104_3384+105del MANE Select	NP_079225.5:n.3384+104_3384+105del