Canonical Allele Identifier: CA2764796796

Gene: WWC2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289756_183289757insACGGTTTGCCAGTCAGTC , CM000666.2:g.183289756_183289757insACGGTTTGCCAGTCAGTC	GRCh38
NC_000004.11:g.184210909_184210910insACGGTTTGCCAGTCAGTC , CM000666.1:g.184210909_184210910insACGGTTTGCCAGTCAGTC	GRCh37
NC_000004.10:g.184447903_184447904insACGGTTTGCCAGTCAGTC	NCBI36
NG_051586.1:g.196122_196123insACGGTTTGCCAGTCAGTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3384+121_3384+122insACGGTTTGCCAGTCAGTC MANE Select	ENSP00000384222.3:n.3384+121_3384+122insACGGTTTGCCAGTCAGTC
ENST00000403733.7:c.3384+121_3384+122insACGGTTTGCCAGTCAGTC	ENSP00000384222.3:n.3384+121_3384+122insACGGTTTGCCAGTCAGTC
ENST00000427431.5:c.*2776+121_*2776+122insACGGTTTGCCAGTCAGTC	ENSP00000393342.1:n.*2776+121_*2776+122insACGGTTTGCCAGTCAGTC
ENST00000438543.5:c.*1180+121_*1180+122insACGGTTTGCCAGTCAGTC	ENSP00000413521.1:n.*1180+121_*1180+122insACGGTTTGCCAGTCAGTC
ENST00000448232.6:c.3456+121_3456+122insACGGTTTGCCAGTCAGTC	ENSP00000398577.2:n.3456+121_3456+122insACGGTTTGCCAGTCAGTC
ENST00000504005.5:c.2430+121_2430+122insACGGTTTGCCAGTCAGTC	ENSP00000427569.1:n.2430+121_2430+122insACGGTTTGCCAGTCAGTC
ENST00000508747.1:c.768+121_768+122insACGGTTTGCCAGTCAGTC	ENSP00000420835.1:n.768+121_768+122insACGGTTTGCCAGTCAGTC
ENST00000513834.5:c.3237+121_3237+122insACGGTTTGCCAGTCAGTC	ENSP00000425054.1:n.3237+121_3237+122insACGGTTTGCCAGTCAGTC
NM_024949.5:c.3384+121_3384+122insACGGTTTGCCAGTCAGTC	NP_079225.5:n.3384+121_3384+122insACGGTTTGCCAGTCAGTC
XM_011532269.1:c.3456+121_3456+122insACGGTTTGCCAGTCAGTC	XP_011530571.1:n.3456+121_3456+122insACGGTTTGCCAGTCAGTC
XM_011532269.3:c.3456+121_3456+122insACGGTTTGCCAGTCAGTC	XP_011530571.1:n.3456+121_3456+122insACGGTTTGCCAGTCAGTC
XM_024454225.1:c.3162+121_3162+122insACGGTTTGCCAGTCAGTC	XP_024309993.1:n.3162+121_3162+122insACGGTTTGCCAGTCAGTC
NM_024949.6:c.3384+121_3384+122insACGGTTTGCCAGTCAGTC MANE Select	NP_079225.5:n.3384+121_3384+122insACGGTTTGCCAGTCAGTC