Canonical Allele Identifier: CA1518546831

Gene: WWC2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289732_183289734delinsTAA , CM000666.2:g.183289732_183289734delinsTAA	GRCh38
NC_000004.11:g.184210885_184210887delinsTAA , CM000666.1:g.184210885_184210887delinsTAA	GRCh37
NC_000004.10:g.184447879_184447881delinsTAA	NCBI36
NG_051586.1:g.196098_196100delinsTAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3384+97_3384+99delinsTAA MANE Select	ENSP00000384222.3:n.3384+97_3384+99delinsTAA
ENST00000403733.7:c.3384+97_3384+99delinsTAA	ENSP00000384222.3:n.3384+97_3384+99delinsTAA
ENST00000427431.5:c.*2776+97_*2776+99delinsTAA	ENSP00000393342.1:n.*2776+97_*2776+99delinsTAA
ENST00000438543.5:c.*1180+97_*1180+99delinsTAA	ENSP00000413521.1:n.*1180+97_*1180+99delinsTAA
ENST00000448232.6:c.3456+97_3456+99delinsTAA	ENSP00000398577.2:n.3456+97_3456+99delinsTAA
ENST00000504005.5:c.2430+97_2430+99delinsTAA	ENSP00000427569.1:n.2430+97_2430+99delinsTAA
ENST00000508747.1:c.768+97_768+99delinsTAA	ENSP00000420835.1:n.768+97_768+99delinsTAA
ENST00000513834.5:c.3237+97_3237+99delinsTAA	ENSP00000425054.1:n.3237+97_3237+99delinsTAA
NM_024949.5:c.3384+97_3384+99delinsTAA	NP_079225.5:n.3384+97_3384+99delinsTAA
XM_011532269.1:c.3456+97_3456+99delinsTAA	XP_011530571.1:n.3456+97_3456+99delinsTAA
XM_011532269.3:c.3456+97_3456+99delinsTAA	XP_011530571.1:n.3456+97_3456+99delinsTAA
XM_024454225.1:c.3162+97_3162+99delinsTAA	XP_024309993.1:n.3162+97_3162+99delinsTAA
NM_024949.6:c.3384+97_3384+99delinsTAA MANE Select	NP_079225.5:n.3384+97_3384+99delinsTAA