Canonical Allele Identifier: CA1518546698
Gene: WWC2 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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