Canonical Allele Identifier: CA1518546742

Gene: WWC2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289531C= , CM000666.2:g.183289531C=	GRCh38
NC_000004.11:g.184210684C= , CM000666.1:g.184210684C=	GRCh37
NC_000004.10:g.184447678C=	NCBI36
NG_051586.1:g.195897C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3280C= MANE Select	ENSP00000384222.3:p.Arg1094=
ENST00000403733.7:c.3280C=	ENSP00000384222.3:p.Arg1094=
ENST00000427431.5:c.*2672C=	ENSP00000393342.1:n.*2672C=
ENST00000438543.5:c.*1076C=	ENSP00000413521.1:n.*1076C=
ENST00000448232.6:c.3352C=	ENSP00000398577.2:p.Arg1118=
ENST00000504005.5:c.2326C=	ENSP00000427569.1:p.Arg776=
ENST00000508747.1:c.664C=	ENSP00000420835.1:p.Arg222=
ENST00000513834.5:c.3133C=	ENSP00000425054.1:p.Arg1045=
NM_024949.5:c.3280C=	NP_079225.5:p.Arg1094=
XM_011532269.1:c.3352C=	XP_011530571.1:p.Arg1118=
XM_011532269.3:c.3352C=	XP_011530571.1:p.Arg1118=
XM_024454225.1:c.3058C=	XP_024309993.1:p.Arg1020=
NM_024949.6:c.3280C= MANE Select	NP_079225.5:p.Arg1094=