Canonical Allele Identifier: CA1518546737

Gene: WWC2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289520T= , CM000666.2:g.183289520T=	GRCh38
NC_000004.11:g.184210673T= , CM000666.1:g.184210673T=	GRCh37
NC_000004.10:g.184447667T=	NCBI36
NG_051586.1:g.195886T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3269T= MANE Select	ENSP00000384222.3:p.Leu1090=
ENST00000403733.7:c.3269T=	ENSP00000384222.3:p.Leu1090=
ENST00000427431.5:c.*2661T=	ENSP00000393342.1:n.*2661T=
ENST00000438543.5:c.*1065T=	ENSP00000413521.1:n.*1065T=
ENST00000448232.6:c.3341T=	ENSP00000398577.2:p.Leu1114=
ENST00000504005.5:c.2315T=	ENSP00000427569.1:p.Leu772=
ENST00000508747.1:c.653T=	ENSP00000420835.1:p.Leu218=
ENST00000513834.5:c.3122T=	ENSP00000425054.1:p.Leu1041=
NM_024949.5:c.3269T=	NP_079225.5:p.Leu1090=
XM_011532269.1:c.3341T=	XP_011530571.1:p.Leu1114=
XM_011532269.3:c.3341T=	XP_011530571.1:p.Leu1114=
XM_024454225.1:c.3047T=	XP_024309993.1:p.Leu1016=
NM_024949.6:c.3269T= MANE Select	NP_079225.5:p.Leu1090=