Canonical Allele Identifier: CA358845877
Gene: WWC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.183289459G>T , CM000666.2:g.183289459G>T GRCh38
NC_000004.11:g.184210612G>T , CM000666.1:g.184210612G>T GRCh37
NC_000004.10:g.184447606G>T NCBI36
NG_051586.1:g.195825G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000403733.8:c.3208G>T MANE Select ENSP00000384222.3:p.Glu1070Ter
ENST00000403733.7:c.3208G>T ENSP00000384222.3:p.Glu1070Ter
ENST00000427431.5:c.*2600G>T ENSP00000393342.1:n.*2600G>T
ENST00000438543.5:c.*1004G>T ENSP00000413521.1:n.*1004G>T
ENST00000448232.6:c.3280G>T ENSP00000398577.2:p.Glu1094Ter
ENST00000504005.5:c.2254G>T ENSP00000427569.1:p.Glu752Ter
ENST00000508747.1:c.592G>T ENSP00000420835.1:p.Glu198Ter
ENST00000513834.5:c.3061G>T ENSP00000425054.1:p.Glu1021Ter
NM_024949.5:c.3208G>T NP_079225.5:p.Glu1070Ter
XM_011532269.1:c.3280G>T XP_011530571.1:p.Glu1094Ter
XM_011532269.3:c.3280G>T XP_011530571.1:p.Glu1094Ter
XM_024454225.1:c.2986G>T XP_024309993.1:p.Glu996Ter
NM_024949.6:c.3208G>T MANE Select NP_079225.5:p.Glu1070Ter