Canonical Allele Identifier: CA1518546721

Gene: WWC2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289491G= , CM000666.2:g.183289491G=	GRCh38
NC_000004.11:g.184210644G= , CM000666.1:g.184210644G=	GRCh37
NC_000004.10:g.184447638G=	NCBI36
NG_051586.1:g.195857G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3240G= MANE Select	ENSP00000384222.3:p.Gln1080=
ENST00000403733.7:c.3240G=	ENSP00000384222.3:p.Gln1080=
ENST00000427431.5:c.*2632G=	ENSP00000393342.1:n.*2632G=
ENST00000438543.5:c.*1036G=	ENSP00000413521.1:n.*1036G=
ENST00000448232.6:c.3312G=	ENSP00000398577.2:p.Gln1104=
ENST00000504005.5:c.2286G=	ENSP00000427569.1:p.Gln762=
ENST00000508747.1:c.624G=	ENSP00000420835.1:p.Gln208=
ENST00000513834.5:c.3093G=	ENSP00000425054.1:p.Gln1031=
NM_024949.5:c.3240G=	NP_079225.5:p.Gln1080=
XM_011532269.1:c.3312G=	XP_011530571.1:p.Gln1104=
XM_011532269.3:c.3312G=	XP_011530571.1:p.Gln1104=
XM_024454225.1:c.3018G=	XP_024309993.1:p.Gln1006=
NM_024949.6:c.3240G= MANE Select	NP_079225.5:p.Gln1080=