Canonical Allele Identifier: CA358846343

Gene: WWC2

Linked Data

• dbSNP Id: rs765691328
• gnomAD v2: 4-184210747-G-A
• gnomAD v3: 4-183289594-G-A
• gnomAD v4: 4-183289594-G-A
• MyVariant Identifiers: chr4:g.184210747G>A (hg19) ; chr4:g.183289594G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289594G>A , CM000666.2:g.183289594G>A	GRCh38
NC_000004.11:g.184210747G>A , CM000666.1:g.184210747G>A	GRCh37
NC_000004.10:g.184447741G>A	NCBI36
NG_051586.1:g.195960G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3343G>A MANE Select	ENSP00000384222.3:p.Asp1115Asn
ENST00000403733.7:c.3343G>A	ENSP00000384222.3:p.Asp1115Asn
ENST00000427431.5:c.*2735G>A	ENSP00000393342.1:n.*2735G>A
ENST00000438543.5:c.*1139G>A	ENSP00000413521.1:n.*1139G>A
ENST00000448232.6:c.3415G>A	ENSP00000398577.2:p.Asp1139Asn
ENST00000504005.5:c.2389G>A	ENSP00000427569.1:p.Asp797Asn
ENST00000508747.1:c.727G>A	ENSP00000420835.1:p.Asp243Asn
ENST00000513834.5:c.3196G>A	ENSP00000425054.1:p.Asp1066Asn
NM_024949.5:c.3343G>A	NP_079225.5:p.Asp1115Asn
XM_011532269.1:c.3415G>A	XP_011530571.1:p.Asp1139Asn
XM_011532269.3:c.3415G>A	XP_011530571.1:p.Asp1139Asn
XM_024454225.1:c.3121G>A	XP_024309993.1:p.Asp1041Asn
NM_024949.6:c.3343G>A MANE Select	NP_079225.5:p.Asp1115Asn