Canonical Allele Identifier: CA1518546697

Gene: WWC2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289438G= , CM000666.2:g.183289438G=	GRCh38
NC_000004.11:g.184210591G= , CM000666.1:g.184210591G=	GRCh37
NC_000004.10:g.184447585G=	NCBI36
NG_051586.1:g.195804G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3187G= MANE Select	ENSP00000384222.3:p.Val1063=
ENST00000403733.7:c.3187G=	ENSP00000384222.3:p.Val1063=
ENST00000427431.5:c.*2579G=	ENSP00000393342.1:n.*2579G=
ENST00000438543.5:c.*983G=	ENSP00000413521.1:n.*983G=
ENST00000448232.6:c.3259G=	ENSP00000398577.2:p.Val1087=
ENST00000504005.5:c.2233G=	ENSP00000427569.1:p.Val745=
ENST00000508747.1:c.571G=	ENSP00000420835.1:p.Val191=
ENST00000513834.5:c.3040G=	ENSP00000425054.1:p.Val1014=
NM_024949.5:c.3187G=	NP_079225.5:p.Val1063=
XM_011532269.1:c.3259G=	XP_011530571.1:p.Val1087=
XM_011532269.3:c.3259G=	XP_011530571.1:p.Val1087=
XM_024454225.1:c.2965G=	XP_024309993.1:p.Val989=
NM_024949.6:c.3187G= MANE Select	NP_079225.5:p.Val1063=