Canonical Allele Identifier: CA358845762
Gene: WWC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.183289430A>C , CM000666.2:g.183289430A>C GRCh38
NC_000004.11:g.184210583A>C , CM000666.1:g.184210583A>C GRCh37
NC_000004.10:g.184447577A>C NCBI36
NG_051586.1:g.195796A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000403733.8:c.3179A>C MANE Select ENSP00000384222.3:p.Glu1060Ala
ENST00000403733.7:c.3179A>C ENSP00000384222.3:p.Glu1060Ala
ENST00000427431.5:c.*2571A>C ENSP00000393342.1:n.*2571A>C
ENST00000438543.5:c.*975A>C ENSP00000413521.1:n.*975A>C
ENST00000448232.6:c.3251A>C ENSP00000398577.2:p.Glu1084Ala
ENST00000504005.5:c.2225A>C ENSP00000427569.1:p.Glu742Ala
ENST00000508747.1:c.563A>C ENSP00000420835.1:p.Glu188Ala
ENST00000513834.5:c.3032A>C ENSP00000425054.1:p.Glu1011Ala
NM_024949.5:c.3179A>C NP_079225.5:p.Glu1060Ala
XM_011532269.1:c.3251A>C XP_011530571.1:p.Glu1084Ala
XM_011532269.3:c.3251A>C XP_011530571.1:p.Glu1084Ala
XM_024454225.1:c.2957A>C XP_024309993.1:p.Glu986Ala
NM_024949.6:c.3179A>C MANE Select NP_079225.5:p.Glu1060Ala