Canonical Allele Identifier: CA1518546731

Gene: WWC2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289505A= , CM000666.2:g.183289505A=	GRCh38
NC_000004.11:g.184210658A= , CM000666.1:g.184210658A=	GRCh37
NC_000004.10:g.184447652A=	NCBI36
NG_051586.1:g.195871A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3254A= MANE Select	ENSP00000384222.3:p.Asp1085=
ENST00000403733.7:c.3254A=	ENSP00000384222.3:p.Asp1085=
ENST00000427431.5:c.*2646A=	ENSP00000393342.1:n.*2646A=
ENST00000438543.5:c.*1050A=	ENSP00000413521.1:n.*1050A=
ENST00000448232.6:c.3326A=	ENSP00000398577.2:p.Asp1109=
ENST00000504005.5:c.2300A=	ENSP00000427569.1:p.Asp767=
ENST00000508747.1:c.638A=	ENSP00000420835.1:p.Asp213=
ENST00000513834.5:c.3107A=	ENSP00000425054.1:p.Asp1036=
NM_024949.5:c.3254A=	NP_079225.5:p.Asp1085=
XM_011532269.1:c.3326A=	XP_011530571.1:p.Asp1109=
XM_011532269.3:c.3326A=	XP_011530571.1:p.Asp1109=
XM_024454225.1:c.3032A=	XP_024309993.1:p.Asp1011=
NM_024949.6:c.3254A= MANE Select	NP_079225.5:p.Asp1085=