Canonical Allele Identifier: CA358845899

Gene: WWC2

Linked Data

• gnomAD v4: 4-183289465-G-A
• MyVariant Identifiers: chr4:g.184210618G>A (hg19) ; chr4:g.183289465G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289465G>A , CM000666.2:g.183289465G>A	GRCh38
NC_000004.11:g.184210618G>A , CM000666.1:g.184210618G>A	GRCh37
NC_000004.10:g.184447612G>A	NCBI36
NG_051586.1:g.195831G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3214G>A MANE Select	ENSP00000384222.3:p.Asp1072Asn
ENST00000403733.7:c.3214G>A	ENSP00000384222.3:p.Asp1072Asn
ENST00000427431.5:c.*2606G>A	ENSP00000393342.1:n.*2606G>A
ENST00000438543.5:c.*1010G>A	ENSP00000413521.1:n.*1010G>A
ENST00000448232.6:c.3286G>A	ENSP00000398577.2:p.Asp1096Asn
ENST00000504005.5:c.2260G>A	ENSP00000427569.1:p.Asp754Asn
ENST00000508747.1:c.598G>A	ENSP00000420835.1:p.Asp200Asn
ENST00000513834.5:c.3067G>A	ENSP00000425054.1:p.Asp1023Asn
NM_024949.5:c.3214G>A	NP_079225.5:p.Asp1072Asn
XM_011532269.1:c.3286G>A	XP_011530571.1:p.Asp1096Asn
XM_011532269.3:c.3286G>A	XP_011530571.1:p.Asp1096Asn
XM_024454225.1:c.2992G>A	XP_024309993.1:p.Asp998Asn
NM_024949.6:c.3214G>A MANE Select	NP_079225.5:p.Asp1072Asn