Canonical Allele Identifier: CA1518546758

Gene: WWC2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289579C= , CM000666.2:g.183289579C=	GRCh38
NC_000004.11:g.184210732C= , CM000666.1:g.184210732C=	GRCh37
NC_000004.10:g.184447726C=	NCBI36
NG_051586.1:g.195945C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3328C= MANE Select	ENSP00000384222.3:p.Pro1110=
ENST00000403733.7:c.3328C=	ENSP00000384222.3:p.Pro1110=
ENST00000427431.5:c.*2720C=	ENSP00000393342.1:n.*2720C=
ENST00000438543.5:c.*1124C=	ENSP00000413521.1:n.*1124C=
ENST00000448232.6:c.3400C=	ENSP00000398577.2:p.Pro1134=
ENST00000504005.5:c.2374C=	ENSP00000427569.1:p.Pro792=
ENST00000508747.1:c.712C=	ENSP00000420835.1:p.Pro238=
ENST00000513834.5:c.3181C=	ENSP00000425054.1:p.Pro1061=
NM_024949.5:c.3328C=	NP_079225.5:p.Pro1110=
XM_011532269.1:c.3400C=	XP_011530571.1:p.Pro1134=
XM_011532269.3:c.3400C=	XP_011530571.1:p.Pro1134=
XM_024454225.1:c.3106C=	XP_024309993.1:p.Pro1036=
NM_024949.6:c.3328C= MANE Select	NP_079225.5:p.Pro1110=