Canonical Allele Identifier: CA111773921

Gene: WWC2

Linked Data

• dbSNP Id: rs745844409
• gnomAD v2: 4-184210917-CAT-C
• gnomAD v3: 4-183289764-CAT-C
• gnomAD v4: 4-183289764-CAT-C
• MyVariant Identifiers: chr4:g.184210918_184210919del (hg19) ; chr4:g.183289765_183289766del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289767_183289768del , CM000666.2:g.183289767_183289768del	GRCh38
NC_000004.11:g.184210920_184210921del , CM000666.1:g.184210920_184210921del	GRCh37
NC_000004.10:g.184447914_184447915del	NCBI36
NG_051586.1:g.196133_196134del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3384+132_3384+133del MANE Select	ENSP00000384222.3:n.3384+132_3384+133del
ENST00000403733.7:c.3384+132_3384+133del	ENSP00000384222.3:n.3384+132_3384+133del
ENST00000427431.5:c.*2776+132_*2776+133del	ENSP00000393342.1:n.*2776+132_*2776+133del
ENST00000438543.5:c.*1180+132_*1180+133del	ENSP00000413521.1:n.*1180+132_*1180+133del
ENST00000448232.6:c.3456+132_3456+133del	ENSP00000398577.2:n.3456+132_3456+133del
ENST00000504005.5:c.2430+132_2430+133del	ENSP00000427569.1:n.2430+132_2430+133del
ENST00000508747.1:c.768+132_768+133del	ENSP00000420835.1:n.768+132_768+133del
ENST00000513834.5:c.3237+132_3237+133del	ENSP00000425054.1:n.3237+132_3237+133del
NM_024949.5:c.3384+132_3384+133del	NP_079225.5:n.3384+132_3384+133del
XM_011532269.1:c.3456+132_3456+133del	XP_011530571.1:n.3456+132_3456+133del
XM_011532269.3:c.3456+132_3456+133del	XP_011530571.1:n.3456+132_3456+133del
XM_024454225.1:c.3162+132_3162+133del	XP_024309993.1:n.3162+132_3162+133del
NM_024949.6:c.3384+132_3384+133del MANE Select	NP_079225.5:n.3384+132_3384+133del