Canonical Allele Identifier: CA358846339
Gene: WWC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.183289592A>G , CM000666.2:g.183289592A>G GRCh38
NC_000004.11:g.184210745A>G , CM000666.1:g.184210745A>G GRCh37
NC_000004.10:g.184447739A>G NCBI36
NG_051586.1:g.195958A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000403733.8:c.3341A>G MANE Select ENSP00000384222.3:p.Glu1114Gly
ENST00000403733.7:c.3341A>G ENSP00000384222.3:p.Glu1114Gly
ENST00000427431.5:c.*2733A>G ENSP00000393342.1:n.*2733A>G
ENST00000438543.5:c.*1137A>G ENSP00000413521.1:n.*1137A>G
ENST00000448232.6:c.3413A>G ENSP00000398577.2:p.Glu1138Gly
ENST00000504005.5:c.2387A>G ENSP00000427569.1:p.Glu796Gly
ENST00000508747.1:c.725A>G ENSP00000420835.1:p.Glu242Gly
ENST00000513834.5:c.3194A>G ENSP00000425054.1:p.Glu1065Gly
NM_024949.5:c.3341A>G NP_079225.5:p.Glu1114Gly
XM_011532269.1:c.3413A>G XP_011530571.1:p.Glu1138Gly
XM_011532269.3:c.3413A>G XP_011530571.1:p.Glu1138Gly
XM_024454225.1:c.3119A>G XP_024309993.1:p.Glu1040Gly
NM_024949.6:c.3341A>G MANE Select NP_079225.5:p.Glu1114Gly