Canonical Allele Identifier: CA1518546701

Gene: WWC2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289446A= , CM000666.2:g.183289446A=	GRCh38
NC_000004.11:g.184210599A= , CM000666.1:g.184210599A=	GRCh37
NC_000004.10:g.184447593A=	NCBI36
NG_051586.1:g.195812A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3195A= MANE Select	ENSP00000384222.3:p.Thr1065=
ENST00000403733.7:c.3195A=	ENSP00000384222.3:p.Thr1065=
ENST00000427431.5:c.*2587A=	ENSP00000393342.1:n.*2587A=
ENST00000438543.5:c.*991A=	ENSP00000413521.1:n.*991A=
ENST00000448232.6:c.3267A=	ENSP00000398577.2:p.Thr1089=
ENST00000504005.5:c.2241A=	ENSP00000427569.1:p.Thr747=
ENST00000508747.1:c.579A=	ENSP00000420835.1:p.Thr193=
ENST00000513834.5:c.3048A=	ENSP00000425054.1:p.Thr1016=
NM_024949.5:c.3195A=	NP_079225.5:p.Thr1065=
XM_011532269.1:c.3267A=	XP_011530571.1:p.Thr1089=
XM_011532269.3:c.3267A=	XP_011530571.1:p.Thr1089=
XM_024454225.1:c.2973A=	XP_024309993.1:p.Thr991=
NM_024949.6:c.3195A= MANE Select	NP_079225.5:p.Thr1065=