Canonical Allele Identifier: CA557393629

Gene: WWC2

Linked Data

• dbSNP Id: rs1240512585
• gnomAD v2: 4-184210654-A-AATG
• gnomAD v4: 4-183289501-A-AATG
• MyVariant Identifiers: chr4:g.184210654_184210655insATG (hg19) ; chr4:g.183289501_183289502insATG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289506_183289508dup , CM000666.2:g.183289506_183289508dup	GRCh38
NC_000004.11:g.184210659_184210661dup , CM000666.1:g.184210659_184210661dup	GRCh37
NC_000004.10:g.184447653_184447655dup	NCBI36
NG_051586.1:g.195872_195874dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3255_3257dup MANE Select	ENSP00000384222.3:p.Asp1085_Glu1086insAsp
ENST00000403733.7:c.3255_3257dup	ENSP00000384222.3:p.Asp1085_Glu1086insAsp
ENST00000427431.5:c.*2647_*2649dup	ENSP00000393342.1:n.*2647_*2649dup
ENST00000438543.5:c.*1051_*1053dup	ENSP00000413521.1:n.*1051_*1053dup
ENST00000448232.6:c.3327_3329dup	ENSP00000398577.2:p.Asp1109_Glu1110insAsp
ENST00000504005.5:c.2301_2303dup	ENSP00000427569.1:p.Asp767_Glu768insAsp
ENST00000508747.1:c.639_641dup	ENSP00000420835.1:p.Asp213_Glu214insAsp
ENST00000513834.5:c.3108_3110dup	ENSP00000425054.1:p.Asp1036_Glu1037insAsp
NM_024949.5:c.3255_3257dup	NP_079225.5:p.Asp1085_Glu1086insAsp
XM_011532269.1:c.3327_3329dup	XP_011530571.1:p.Asp1109_Glu1110insAsp
XM_011532269.3:c.3327_3329dup	XP_011530571.1:p.Asp1109_Glu1110insAsp
XM_024454225.1:c.3033_3035dup	XP_024309993.1:p.Asp1011_Glu1012insAsp
NM_024949.6:c.3255_3257dup MANE Select	NP_079225.5:p.Asp1085_Glu1086insAsp