Canonical Allele Identifier: CA1518546844

Gene: WWC2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289751C= , CM000666.2:g.183289751C=	GRCh38
NC_000004.11:g.184210904C= , CM000666.1:g.184210904C=	GRCh37
NC_000004.10:g.184447898C=	NCBI36
NG_051586.1:g.196117C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3384+116C= MANE Select	ENSP00000384222.3:n.3384+116C=
ENST00000403733.7:c.3384+116C=	ENSP00000384222.3:n.3384+116C=
ENST00000427431.5:c.*2776+116C=	ENSP00000393342.1:n.*2776+116C=
ENST00000438543.5:c.*1180+116C=	ENSP00000413521.1:n.*1180+116C=
ENST00000448232.6:c.3456+116C=	ENSP00000398577.2:n.3456+116C=
ENST00000504005.5:c.2430+116C=	ENSP00000427569.1:n.2430+116C=
ENST00000508747.1:c.768+116C=	ENSP00000420835.1:n.768+116C=
ENST00000513834.5:c.3237+116C=	ENSP00000425054.1:n.3237+116C=
NM_024949.5:c.3384+116C=	NP_079225.5:n.3384+116C=
XM_011532269.1:c.3456+116C=	XP_011530571.1:n.3456+116C=
XM_011532269.3:c.3456+116C=	XP_011530571.1:n.3456+116C=
XM_024454225.1:c.3162+116C=	XP_024309993.1:n.3162+116C=
NM_024949.6:c.3384+116C= MANE Select	NP_079225.5:n.3384+116C=