Canonical Allele Identifier: CA442557546

Gene: WWC2

Linked Data

• MyVariant Identifiers: chr4:g.184210594C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289441C>A , CM000666.2:g.183289441C>A	GRCh38
NC_000004.11:g.184210594C>A , CM000666.1:g.184210594C>A	GRCh37
NC_000004.10:g.184447588C>A	NCBI36
NG_051586.1:g.195807C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3190C>A MANE Select	ENSP00000384222.3:p.Arg1064=
ENST00000403733.7:c.3190C>A	ENSP00000384222.3:p.Arg1064=
ENST00000427431.5:c.*2582C>A	ENSP00000393342.1:n.*2582C>A
ENST00000438543.5:c.*986C>A	ENSP00000413521.1:n.*986C>A
ENST00000448232.6:c.3262C>A	ENSP00000398577.2:p.Arg1088=
ENST00000504005.5:c.2236C>A	ENSP00000427569.1:p.Arg746=
ENST00000508747.1:c.574C>A	ENSP00000420835.1:p.Arg192=
ENST00000513834.5:c.3043C>A	ENSP00000425054.1:p.Arg1015=
NM_024949.5:c.3190C>A	NP_079225.5:p.Arg1064=
XM_011532269.1:c.3262C>A	XP_011530571.1:p.Arg1088=
XM_011532269.3:c.3262C>A	XP_011530571.1:p.Arg1088=
XM_024454225.1:c.2968C>A	XP_024309993.1:p.Arg990=
NM_024949.6:c.3190C>A MANE Select	NP_079225.5:p.Arg1064=