Canonical Allele Identifier: CA1518546740

Gene: WWC2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289529T= , CM000666.2:g.183289529T=	GRCh38
NC_000004.11:g.184210682T= , CM000666.1:g.184210682T=	GRCh37
NC_000004.10:g.184447676T=	NCBI36
NG_051586.1:g.195895T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3278T= MANE Select	ENSP00000384222.3:p.Leu1093=
ENST00000403733.7:c.3278T=	ENSP00000384222.3:p.Leu1093=
ENST00000427431.5:c.*2670T=	ENSP00000393342.1:n.*2670T=
ENST00000438543.5:c.*1074T=	ENSP00000413521.1:n.*1074T=
ENST00000448232.6:c.3350T=	ENSP00000398577.2:p.Leu1117=
ENST00000504005.5:c.2324T=	ENSP00000427569.1:p.Leu775=
ENST00000508747.1:c.662T=	ENSP00000420835.1:p.Leu221=
ENST00000513834.5:c.3131T=	ENSP00000425054.1:p.Leu1044=
NM_024949.5:c.3278T=	NP_079225.5:p.Leu1093=
XM_011532269.1:c.3350T=	XP_011530571.1:p.Leu1117=
XM_011532269.3:c.3350T=	XP_011530571.1:p.Leu1117=
XM_024454225.1:c.3056T=	XP_024309993.1:p.Leu1019=
NM_024949.6:c.3278T= MANE Select	NP_079225.5:p.Leu1093=