Canonical Allele Identifier: CA1518546707

Gene: WWC2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289464G= , CM000666.2:g.183289464G=	GRCh38
NC_000004.11:g.184210617G= , CM000666.1:g.184210617G=	GRCh37
NC_000004.10:g.184447611G=	NCBI36
NG_051586.1:g.195830G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3213G= MANE Select	ENSP00000384222.3:p.Leu1071=
ENST00000403733.7:c.3213G=	ENSP00000384222.3:p.Leu1071=
ENST00000427431.5:c.*2605G=	ENSP00000393342.1:n.*2605G=
ENST00000438543.5:c.*1009G=	ENSP00000413521.1:n.*1009G=
ENST00000448232.6:c.3285G=	ENSP00000398577.2:p.Leu1095=
ENST00000504005.5:c.2259G=	ENSP00000427569.1:p.Leu753=
ENST00000508747.1:c.597G=	ENSP00000420835.1:p.Leu199=
ENST00000513834.5:c.3066G=	ENSP00000425054.1:p.Leu1022=
NM_024949.5:c.3213G=	NP_079225.5:p.Leu1071=
XM_011532269.1:c.3285G=	XP_011530571.1:p.Leu1095=
XM_011532269.3:c.3285G=	XP_011530571.1:p.Leu1095=
XM_024454225.1:c.2991G=	XP_024309993.1:p.Leu997=
NM_024949.6:c.3213G= MANE Select	NP_079225.5:p.Leu1071=