Canonical Allele Identifier: CA557393628

Gene: WWC2

Linked Data

• dbSNP Id: rs1193042903
• gnomAD v2: 4-184210653-CAAT-C
• gnomAD v4: 4-183289500-CAAT-C
• MyVariant Identifiers: chr4:g.184210654_184210656del (hg19) ; chr4:g.183289501_183289503del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289501_183289503del , CM000666.2:g.183289501_183289503del	GRCh38
NC_000004.11:g.184210654_184210656del , CM000666.1:g.184210654_184210656del	GRCh37
NC_000004.10:g.184447648_184447650del	NCBI36
NG_051586.1:g.195867_195869del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3250_3252del MANE Select	ENSP00000384222.3:p.Asn1084del
ENST00000403733.7:c.3250_3252del	ENSP00000384222.3:p.Asn1084del
ENST00000427431.5:c.*2642_*2644del	ENSP00000393342.1:n.*2642_*2644del
ENST00000438543.5:c.*1046_*1048del	ENSP00000413521.1:n.*1046_*1048del
ENST00000448232.6:c.3322_3324del	ENSP00000398577.2:p.Asn1108del
ENST00000504005.5:c.2296_2298del	ENSP00000427569.1:p.Asn766del
ENST00000508747.1:c.634_636del	ENSP00000420835.1:p.Asn212del
ENST00000513834.5:c.3103_3105del	ENSP00000425054.1:p.Asn1035del
NM_024949.5:c.3250_3252del	NP_079225.5:p.Asn1084del
XM_011532269.1:c.3322_3324del	XP_011530571.1:p.Asn1108del
XM_011532269.3:c.3322_3324del	XP_011530571.1:p.Asn1108del
XM_024454225.1:c.3028_3030del	XP_024309993.1:p.Asn1010del
NM_024949.6:c.3250_3252del MANE Select	NP_079225.5:p.Asn1084del