Canonical Allele Identifier: CA1518546695

Gene: WWC2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289436C= , CM000666.2:g.183289436C=	GRCh38
NC_000004.11:g.184210589C= , CM000666.1:g.184210589C=	GRCh37
NC_000004.10:g.184447583C=	NCBI36
NG_051586.1:g.195802C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3185C= MANE Select	ENSP00000384222.3:p.Pro1062=
ENST00000403733.7:c.3185C=	ENSP00000384222.3:p.Pro1062=
ENST00000427431.5:c.*2577C=	ENSP00000393342.1:n.*2577C=
ENST00000438543.5:c.*981C=	ENSP00000413521.1:n.*981C=
ENST00000448232.6:c.3257C=	ENSP00000398577.2:p.Pro1086=
ENST00000504005.5:c.2231C=	ENSP00000427569.1:p.Pro744=
ENST00000508747.1:c.569C=	ENSP00000420835.1:p.Pro190=
ENST00000513834.5:c.3038C=	ENSP00000425054.1:p.Pro1013=
NM_024949.5:c.3185C=	NP_079225.5:p.Pro1062=
XM_011532269.1:c.3257C=	XP_011530571.1:p.Pro1086=
XM_011532269.3:c.3257C=	XP_011530571.1:p.Pro1086=
XM_024454225.1:c.2963C=	XP_024309993.1:p.Pro988=
NM_024949.6:c.3185C= MANE Select	NP_079225.5:p.Pro1062=