Canonical Allele Identifier: CA1518546756

Gene: WWC2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289576C= , CM000666.2:g.183289576C=	GRCh38
NC_000004.11:g.184210729C= , CM000666.1:g.184210729C=	GRCh37
NC_000004.10:g.184447723C=	NCBI36
NG_051586.1:g.195942C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3325C= MANE Select	ENSP00000384222.3:p.Pro1109=
ENST00000403733.7:c.3325C=	ENSP00000384222.3:p.Pro1109=
ENST00000427431.5:c.*2717C=	ENSP00000393342.1:n.*2717C=
ENST00000438543.5:c.*1121C=	ENSP00000413521.1:n.*1121C=
ENST00000448232.6:c.3397C=	ENSP00000398577.2:p.Pro1133=
ENST00000504005.5:c.2371C=	ENSP00000427569.1:p.Pro791=
ENST00000508747.1:c.709C=	ENSP00000420835.1:p.Pro237=
ENST00000513834.5:c.3178C=	ENSP00000425054.1:p.Pro1060=
NM_024949.5:c.3325C=	NP_079225.5:p.Pro1109=
XM_011532269.1:c.3397C=	XP_011530571.1:p.Pro1133=
XM_011532269.3:c.3397C=	XP_011530571.1:p.Pro1133=
XM_024454225.1:c.3103C=	XP_024309993.1:p.Pro1035=
NM_024949.6:c.3325C= MANE Select	NP_079225.5:p.Pro1109=