Canonical Allele Identifier: CA1518546687

Gene: WWC2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289401C= , CM000666.2:g.183289401C=	GRCh38
NC_000004.11:g.184210554C= , CM000666.1:g.184210554C=	GRCh37
NC_000004.10:g.184447548C=	NCBI36
NG_051586.1:g.195767C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3150C= MANE Select	ENSP00000384222.3:p.Cys1050=
ENST00000403733.7:c.3150C=	ENSP00000384222.3:p.Cys1050=
ENST00000427431.5:c.*2542C=	ENSP00000393342.1:n.*2542C=
ENST00000438543.5:c.*946C=	ENSP00000413521.1:n.*946C=
ENST00000448232.6:c.3222C=	ENSP00000398577.2:p.Cys1074=
ENST00000504005.5:c.2196C=	ENSP00000427569.1:p.Cys732=
ENST00000508747.1:c.534C=	ENSP00000420835.1:p.Cys178=
ENST00000513834.5:c.3003C=	ENSP00000425054.1:p.Cys1001=
NM_024949.5:c.3150C=	NP_079225.5:p.Cys1050=
XM_011532269.1:c.3222C=	XP_011530571.1:p.Cys1074=
XM_011532269.3:c.3222C=	XP_011530571.1:p.Cys1074=
XM_024454225.1:c.2928C=	XP_024309993.1:p.Cys976=
NM_024949.6:c.3150C= MANE Select	NP_079225.5:p.Cys1050=