Canonical Allele Identifier: CA2764796792

Gene: WWC2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289745_183289746insGGTAACCACTGCCTGTATAACCAGGGTG , CM000666.2:g.183289745_183289746insGGTAACCACTGCCTGTATAACCAGGGTG	GRCh38
NC_000004.11:g.184210898_184210899insGGTAACCACTGCCTGTATAACCAGGGTG , CM000666.1:g.184210898_184210899insGGTAACCACTGCCTGTATAACCAGGGTG	GRCh37
NC_000004.10:g.184447892_184447893insGGTAACCACTGCCTGTATAACCAGGGTG	NCBI36
NG_051586.1:g.196111_196112insGGTAACCACTGCCTGTATAACCAGGGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3384+110_3384+111insGGTAACCACTGCCTGTATAACCAGGGTG MANE Select	ENSP00000384222.3:n.3384+110_3384+111insGGTAACCACTGCCTGTATAAC...
ENST00000403733.7:c.3384+110_3384+111insGGTAACCACTGCCTGTATAACCAGGGTG	ENSP00000384222.3:n.3384+110_3384+111insGGTAACCACTGCCTGTATAAC...
ENST00000427431.5:c.*2776+110_*2776+111insGGTAACCACTGCCTGTATAACCAGGGTG	ENSP00000393342.1:n.*2776+110_*2776+111insGGTAACCACTGCCTGTATA...
ENST00000438543.5:c.*1180+110_*1180+111insGGTAACCACTGCCTGTATAACCAGGGTG	ENSP00000413521.1:n.*1180+110_*1180+111insGGTAACCACTGCCTGTATA...
ENST00000448232.6:c.3456+110_3456+111insGGTAACCACTGCCTGTATAACCAGGGTG	ENSP00000398577.2:n.3456+110_3456+111insGGTAACCACTGCCTGTATAAC...
ENST00000504005.5:c.2430+110_2430+111insGGTAACCACTGCCTGTATAACCAGGGTG	ENSP00000427569.1:n.2430+110_2430+111insGGTAACCACTGCCTGTATAAC...
ENST00000508747.1:c.768+110_768+111insGGTAACCACTGCCTGTATAACCAGGGTG	ENSP00000420835.1:n.768+110_768+111insGGTAACCACTGCCTGTATAACCA...
ENST00000513834.5:c.3237+110_3237+111insGGTAACCACTGCCTGTATAACCAGGGTG	ENSP00000425054.1:n.3237+110_3237+111insGGTAACCACTGCCTGTATAAC...
NM_024949.5:c.3384+110_3384+111insGGTAACCACTGCCTGTATAACCAGGGTG	NP_079225.5:n.3384+110_3384+111insGGTAACCACTGCCTGTATAACCAGGGT...
XM_011532269.1:c.3456+110_3456+111insGGTAACCACTGCCTGTATAACCAGGGTG	XP_011530571.1:n.3456+110_3456+111insGGTAACCACTGCCTGTATAACCAG...
XM_011532269.3:c.3456+110_3456+111insGGTAACCACTGCCTGTATAACCAGGGTG	XP_011530571.1:n.3456+110_3456+111insGGTAACCACTGCCTGTATAACCAG...
XM_024454225.1:c.3162+110_3162+111insGGTAACCACTGCCTGTATAACCAGGGTG	XP_024309993.1:n.3162+110_3162+111insGGTAACCACTGCCTGTATAACCAG...
NM_024949.6:c.3384+110_3384+111insGGTAACCACTGCCTGTATAACCAGGGTG MANE Select	NP_079225.5:n.3384+110_3384+111insGGTAACCACTGCCTGTATAACCAGGGT...