Canonical Allele Identifier: CA358845768

Gene: WWC2

Linked Data

• MyVariant Identifiers: chr4:g.184210585T>A (hg19) ; chr4:g.183289432T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289432T>A , CM000666.2:g.183289432T>A	GRCh38
NC_000004.11:g.184210585T>A , CM000666.1:g.184210585T>A	GRCh37
NC_000004.10:g.184447579T>A	NCBI36
NG_051586.1:g.195798T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3181T>A MANE Select	ENSP00000384222.3:p.Cys1061Ser
ENST00000403733.7:c.3181T>A	ENSP00000384222.3:p.Cys1061Ser
ENST00000427431.5:c.*2573T>A	ENSP00000393342.1:n.*2573T>A
ENST00000438543.5:c.*977T>A	ENSP00000413521.1:n.*977T>A
ENST00000448232.6:c.3253T>A	ENSP00000398577.2:p.Cys1085Ser
ENST00000504005.5:c.2227T>A	ENSP00000427569.1:p.Cys743Ser
ENST00000508747.1:c.565T>A	ENSP00000420835.1:p.Cys189Ser
ENST00000513834.5:c.3034T>A	ENSP00000425054.1:p.Cys1012Ser
NM_024949.5:c.3181T>A	NP_079225.5:p.Cys1061Ser
XM_011532269.1:c.3253T>A	XP_011530571.1:p.Cys1085Ser
XM_011532269.3:c.3253T>A	XP_011530571.1:p.Cys1085Ser
XM_024454225.1:c.2959T>A	XP_024309993.1:p.Cys987Ser
NM_024949.6:c.3181T>A MANE Select	NP_079225.5:p.Cys1061Ser