Canonical Allele Identifier: CA1518546573

Gene: WWC2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289145T= , CM000666.2:g.183289145T=	GRCh38
NC_000004.11:g.184210298T= , CM000666.1:g.184210298T=	GRCh37
NC_000004.10:g.184447292T=	NCBI36
NG_051586.1:g.195511T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3142-248T= MANE Select	ENSP00000384222.3:n.3142-248T=
ENST00000403733.7:c.3142-248T=	ENSP00000384222.3:n.3142-248T=
ENST00000427431.5:c.*2534-248T=	ENSP00000393342.1:n.*2534-248T=
ENST00000438543.5:c.*938-248T=	ENSP00000413521.1:n.*938-248T=
ENST00000448232.6:c.3214-248T=	ENSP00000398577.2:n.3214-248T=
ENST00000504005.5:c.2188-248T=	ENSP00000427569.1:n.2188-248T=
ENST00000508747.1:c.526-248T=	ENSP00000420835.1:n.526-248T=
ENST00000513834.5:c.2995-248T=	ENSP00000425054.1:n.2995-248T=
NM_024949.5:c.3142-248T=	NP_079225.5:n.3142-248T=
XM_011532269.1:c.3214-248T=	XP_011530571.1:n.3214-248T=
XM_011532269.3:c.3214-248T=	XP_011530571.1:n.3214-248T=
XM_024454225.1:c.2920-248T=	XP_024309993.1:n.2920-248T=
NM_024949.6:c.3142-248T= MANE Select	NP_079225.5:n.3142-248T=