Canonical Allele Identifier: CA358845829

Gene: WWC2

Linked Data

• gnomAD v4: 4-183289448-C-A
• COSMIC: COSM5515029 ; COSM5515030 ; COSM5515031
• MyVariant Identifiers: chr4:g.184210601C>A (hg19) ; chr4:g.183289448C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289448C>A , CM000666.2:g.183289448C>A	GRCh38
NC_000004.11:g.184210601C>A , CM000666.1:g.184210601C>A	GRCh37
NC_000004.10:g.184447595C>A	NCBI36
NG_051586.1:g.195814C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3197C>A MANE Select	ENSP00000384222.3:p.Ser1066Tyr
ENST00000403733.7:c.3197C>A	ENSP00000384222.3:p.Ser1066Tyr
ENST00000427431.5:c.*2589C>A	ENSP00000393342.1:n.*2589C>A
ENST00000438543.5:c.*993C>A	ENSP00000413521.1:n.*993C>A
ENST00000448232.6:c.3269C>A	ENSP00000398577.2:p.Ser1090Tyr
ENST00000504005.5:c.2243C>A	ENSP00000427569.1:p.Ser748Tyr
ENST00000508747.1:c.581C>A	ENSP00000420835.1:p.Ser194Tyr
ENST00000513834.5:c.3050C>A	ENSP00000425054.1:p.Ser1017Tyr
NM_024949.5:c.3197C>A	NP_079225.5:p.Ser1066Tyr
XM_011532269.1:c.3269C>A	XP_011530571.1:p.Ser1090Tyr
XM_011532269.3:c.3269C>A	XP_011530571.1:p.Ser1090Tyr
XM_024454225.1:c.2975C>A	XP_024309993.1:p.Ser992Tyr
NM_024949.6:c.3197C>A MANE Select	NP_079225.5:p.Ser1066Tyr