Canonical Allele Identifier: CA1518546869

Gene: WWC2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289808_183289809delinsAC , CM000666.2:g.183289808_183289809delinsAC	GRCh38
NC_000004.11:g.184210961_184210962delinsAC , CM000666.1:g.184210961_184210962delinsAC	GRCh37
NC_000004.10:g.184447955_184447956delinsAC	NCBI36
NG_051586.1:g.196174_196175delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3384+173_3384+174delinsAC MANE Select	ENSP00000384222.3:n.3384+173_3384+174delinsAC
ENST00000403733.7:c.3384+173_3384+174delinsAC	ENSP00000384222.3:n.3384+173_3384+174delinsAC
ENST00000427431.5:c.*2776+173_*2776+174delinsAC	ENSP00000393342.1:n.*2776+173_*2776+174delinsAC
ENST00000438543.5:c.*1180+173_*1180+174delinsAC	ENSP00000413521.1:n.*1180+173_*1180+174delinsAC
ENST00000448232.6:c.3456+173_3456+174delinsAC	ENSP00000398577.2:n.3456+173_3456+174delinsAC
ENST00000504005.5:c.2430+173_2430+174delinsAC	ENSP00000427569.1:n.2430+173_2430+174delinsAC
ENST00000508747.1:c.768+173_768+174delinsAC	ENSP00000420835.1:n.768+173_768+174delinsAC
ENST00000513834.5:c.3237+173_3237+174delinsAC	ENSP00000425054.1:n.3237+173_3237+174delinsAC
NM_024949.5:c.3384+173_3384+174delinsAC	NP_079225.5:n.3384+173_3384+174delinsAC
XM_011532269.1:c.3456+173_3456+174delinsAC	XP_011530571.1:n.3456+173_3456+174delinsAC
XM_011532269.3:c.3456+173_3456+174delinsAC	XP_011530571.1:n.3456+173_3456+174delinsAC
XM_024454225.1:c.3162+173_3162+174delinsAC	XP_024309993.1:n.3162+173_3162+174delinsAC
NM_024949.6:c.3384+173_3384+174delinsAC MANE Select	NP_079225.5:n.3384+173_3384+174delinsAC