Canonical Allele Identifier: CA1518546541

Gene: WWC2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289072_183289073delinsAG , CM000666.2:g.183289072_183289073delinsAG	GRCh38
NC_000004.11:g.184210225_184210226delinsAG , CM000666.1:g.184210225_184210226delinsAG	GRCh37
NC_000004.10:g.184447219_184447220delinsAG	NCBI36
NG_051586.1:g.195438_195439delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3142-321_3142-320delinsAG MANE Select	ENSP00000384222.3:n.3142-321_3142-320delinsAG
ENST00000403733.7:c.3142-321_3142-320delinsAG	ENSP00000384222.3:n.3142-321_3142-320delinsAG
ENST00000427431.5:c.*2534-321_*2534-320delinsAG	ENSP00000393342.1:n.*2534-321_*2534-320delinsAG
ENST00000438543.5:c.*938-321_*938-320delinsAG	ENSP00000413521.1:n.*938-321_*938-320delinsAG
ENST00000448232.6:c.3214-321_3214-320delinsAG	ENSP00000398577.2:n.3214-321_3214-320delinsAG
ENST00000504005.5:c.2188-321_2188-320delinsAG	ENSP00000427569.1:n.2188-321_2188-320delinsAG
ENST00000508747.1:c.526-321_526-320delinsAG	ENSP00000420835.1:n.526-321_526-320delinsAG
ENST00000513834.5:c.2995-321_2995-320delinsAG	ENSP00000425054.1:n.2995-321_2995-320delinsAG
NM_024949.5:c.3142-321_3142-320delinsAG	NP_079225.5:n.3142-321_3142-320delinsAG
XM_011532269.1:c.3214-321_3214-320delinsAG	XP_011530571.1:n.3214-321_3214-320delinsAG
XM_011532269.3:c.3214-321_3214-320delinsAG	XP_011530571.1:n.3214-321_3214-320delinsAG
XM_024454225.1:c.2920-321_2920-320delinsAG	XP_024309993.1:n.2920-321_2920-320delinsAG
NM_024949.6:c.3142-321_3142-320delinsAG MANE Select	NP_079225.5:n.3142-321_3142-320delinsAG