Canonical Allele Identifier: CA1518546558

Gene: WWC2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289102T= , CM000666.2:g.183289102T=	GRCh38
NC_000004.11:g.184210255T= , CM000666.1:g.184210255T=	GRCh37
NC_000004.10:g.184447249T=	NCBI36
NG_051586.1:g.195468T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3142-291T= MANE Select	ENSP00000384222.3:n.3142-291T=
ENST00000403733.7:c.3142-291T=	ENSP00000384222.3:n.3142-291T=
ENST00000427431.5:c.*2534-291T=	ENSP00000393342.1:n.*2534-291T=
ENST00000438543.5:c.*938-291T=	ENSP00000413521.1:n.*938-291T=
ENST00000448232.6:c.3214-291T=	ENSP00000398577.2:n.3214-291T=
ENST00000504005.5:c.2188-291T=	ENSP00000427569.1:n.2188-291T=
ENST00000508747.1:c.526-291T=	ENSP00000420835.1:n.526-291T=
ENST00000513834.5:c.2995-291T=	ENSP00000425054.1:n.2995-291T=
NM_024949.5:c.3142-291T=	NP_079225.5:n.3142-291T=
XM_011532269.1:c.3214-291T=	XP_011530571.1:n.3214-291T=
XM_011532269.3:c.3214-291T=	XP_011530571.1:n.3214-291T=
XM_024454225.1:c.2920-291T=	XP_024309993.1:n.2920-291T=
NM_024949.6:c.3142-291T= MANE Select	NP_079225.5:n.3142-291T=