Canonical Allele Identifier: CA1518546727

Gene: WWC2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289500_183289503delinsCAAT , CM000666.2:g.183289500_183289503delinsCAAT	GRCh38
NC_000004.11:g.184210653_184210656delinsCAAT , CM000666.1:g.184210653_184210656delinsCAAT	GRCh37
NC_000004.10:g.184447647_184447650delinsCAAT	NCBI36
NG_051586.1:g.195866_195869delinsCAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3249_3252delinsCAAT MANE Select	ENSP00000384222.3:p.Leu1083=
ENST00000403733.7:c.3249_3252delinsCAAT	ENSP00000384222.3:p.Leu1083=
ENST00000427431.5:c.*2641_*2644delinsCAAT	ENSP00000393342.1:n.*2641_*2644delinsCAAT
ENST00000438543.5:c.*1045_*1048delinsCAAT	ENSP00000413521.1:n.*1045_*1048delinsCAAT
ENST00000448232.6:c.3321_3324delinsCAAT	ENSP00000398577.2:p.Leu1107=
ENST00000504005.5:c.2295_2298delinsCAAT	ENSP00000427569.1:p.Leu765=
ENST00000508747.1:c.633_636delinsCAAT	ENSP00000420835.1:p.Leu211=
ENST00000513834.5:c.3102_3105delinsCAAT	ENSP00000425054.1:p.Leu1034=
NM_024949.5:c.3249_3252delinsCAAT	NP_079225.5:p.Leu1083=
XM_011532269.1:c.3321_3324delinsCAAT	XP_011530571.1:p.Leu1107=
XM_011532269.3:c.3321_3324delinsCAAT	XP_011530571.1:p.Leu1107=
XM_024454225.1:c.3027_3030delinsCAAT	XP_024309993.1:p.Leu1009=
NM_024949.6:c.3249_3252delinsCAAT MANE Select	NP_079225.5:p.Leu1083=