Canonical Allele Identifier: CA1518546711

Gene: WWC2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289470T= , CM000666.2:g.183289470T=	GRCh38
NC_000004.11:g.184210623T= , CM000666.1:g.184210623T=	GRCh37
NC_000004.10:g.184447617T=	NCBI36
NG_051586.1:g.195836T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3219T= MANE Select	ENSP00000384222.3:p.Leu1073=
ENST00000403733.7:c.3219T=	ENSP00000384222.3:p.Leu1073=
ENST00000427431.5:c.*2611T=	ENSP00000393342.1:n.*2611T=
ENST00000438543.5:c.*1015T=	ENSP00000413521.1:n.*1015T=
ENST00000448232.6:c.3291T=	ENSP00000398577.2:p.Leu1097=
ENST00000504005.5:c.2265T=	ENSP00000427569.1:p.Leu755=
ENST00000508747.1:c.603T=	ENSP00000420835.1:p.Leu201=
ENST00000513834.5:c.3072T=	ENSP00000425054.1:p.Leu1024=
NM_024949.5:c.3219T=	NP_079225.5:p.Leu1073=
XM_011532269.1:c.3291T=	XP_011530571.1:p.Leu1097=
XM_011532269.3:c.3291T=	XP_011530571.1:p.Leu1097=
XM_024454225.1:c.2997T=	XP_024309993.1:p.Leu999=
NM_024949.6:c.3219T= MANE Select	NP_079225.5:p.Leu1073=