Canonical Allele Identifier: CA358845728

Gene: WWC2

Linked Data

• gnomAD v4: 4-183289418-G-T
• MyVariant Identifiers: chr4:g.184210571G>T (hg19) ; chr4:g.183289418G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289418G>T , CM000666.2:g.183289418G>T	GRCh38
NC_000004.11:g.184210571G>T , CM000666.1:g.184210571G>T	GRCh37
NC_000004.10:g.184447565G>T	NCBI36
NG_051586.1:g.195784G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3167G>T MANE Select	ENSP00000384222.3:p.Arg1056Ile
ENST00000403733.7:c.3167G>T	ENSP00000384222.3:p.Arg1056Ile
ENST00000427431.5:c.*2559G>T	ENSP00000393342.1:n.*2559G>T
ENST00000438543.5:c.*963G>T	ENSP00000413521.1:n.*963G>T
ENST00000448232.6:c.3239G>T	ENSP00000398577.2:p.Arg1080Ile
ENST00000504005.5:c.2213G>T	ENSP00000427569.1:p.Arg738Ile
ENST00000508747.1:c.551G>T	ENSP00000420835.1:p.Arg184Ile
ENST00000513834.5:c.3020G>T	ENSP00000425054.1:p.Arg1007Ile
NM_024949.5:c.3167G>T	NP_079225.5:p.Arg1056Ile
XM_011532269.1:c.3239G>T	XP_011530571.1:p.Arg1080Ile
XM_011532269.3:c.3239G>T	XP_011530571.1:p.Arg1080Ile
XM_024454225.1:c.2945G>T	XP_024309993.1:p.Arg982Ile
NM_024949.6:c.3167G>T MANE Select	NP_079225.5:p.Arg1056Ile