Canonical Allele Identifier: CA917381730

Gene: WWC2

Linked Data

• dbSNP Id: rs1560889196

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289803_183289804insTTC , CM000666.2:g.183289803_183289804insTTC	GRCh38
NC_000004.11:g.184210956_184210957insTTC , CM000666.1:g.184210956_184210957insTTC	GRCh37
NC_000004.10:g.184447950_184447951insTTC	NCBI36
NG_051586.1:g.196169_196170insTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3384+168_3384+169insTTC MANE Select	ENSP00000384222.3:n.3384+168_3384+169insTTC
ENST00000403733.7:c.3384+168_3384+169insTTC	ENSP00000384222.3:n.3384+168_3384+169insTTC
ENST00000427431.5:c.*2776+168_*2776+169insTTC	ENSP00000393342.1:n.*2776+168_*2776+169insTTC
ENST00000438543.5:c.*1180+168_*1180+169insTTC	ENSP00000413521.1:n.*1180+168_*1180+169insTTC
ENST00000448232.6:c.3456+168_3456+169insTTC	ENSP00000398577.2:n.3456+168_3456+169insTTC
ENST00000504005.5:c.2430+168_2430+169insTTC	ENSP00000427569.1:n.2430+168_2430+169insTTC
ENST00000508747.1:c.768+168_768+169insTTC	ENSP00000420835.1:n.768+168_768+169insTTC
ENST00000513834.5:c.3237+168_3237+169insTTC	ENSP00000425054.1:n.3237+168_3237+169insTTC
NM_024949.5:c.3384+168_3384+169insTTC	NP_079225.5:n.3384+168_3384+169insTTC
XM_011532269.1:c.3456+168_3456+169insTTC	XP_011530571.1:n.3456+168_3456+169insTTC
XM_011532269.3:c.3456+168_3456+169insTTC	XP_011530571.1:n.3456+168_3456+169insTTC
XM_024454225.1:c.3162+168_3162+169insTTC	XP_024309993.1:n.3162+168_3162+169insTTC
NM_024949.6:c.3384+168_3384+169insTTC MANE Select	NP_079225.5:n.3384+168_3384+169insTTC