Canonical Allele Identifier: CA1928998436
Gene: PLCE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94298552G= , CM000672.2:g.94298552G= GRCh38
NC_000010.10:g.96058309G= , CM000672.1:g.96058309G= GRCh37
NC_000010.9:g.96048299G= NCBI36
NG_015799.1:g.309564G=

Transcript Alleles

HGVS Amino-acid change
ENST00000371380.8:c.5341G= MANE Select ENSP00000360431.2:p.Ala1781=
ENST00000371385.8:c.4315G= ENSP00000360438.4:p.Ala1439=
ENST00000674738.1:n.3896G=
ENST00000674827.1:n.3457G= ENSP00000502523.1:p.Ala1153=
ENST00000675218.1:n.4417G= ENSP00000501910.1:p.Ala1473=
ENST00000675487.1:c.*1274G= ENSP00000502340.1:p.=
ENST00000675718.1:n.4610G=
ENST00000260766.7:c.5341G= ENSP00000260766.3:p.Ala1781=
ENST00000371375.1:n.4417G= ENSP00000360426.1:p.Ala1473=
ENST00000371380.7:c.5341G= ENSP00000360431.2:p.Ala1781=
ENST00000371385.7:c.4417G= ENSP00000360438.3:p.Ala1473=
NM_001165979.2:c.4417G= NP_001159451.1:p.Ala1473=
NM_001288989.1:c.5293G= NP_001275918.1:p.Ala1765=
NM_016341.3:c.5341G= NP_057425.3:p.Ala1781=
XM_006717885.2:c.5383G= XP_006717948.1:p.Ala1795=
XM_006717886.2:c.5383G= XP_006717949.1:p.Ala1795=
XM_006717888.2:c.5380G= XP_006717951.1:p.Ala1794=
XM_006717889.2:c.5335G= XP_006717952.1:p.Ala1779=
XM_006717890.1:c.4459G= XP_006717953.1:p.Ala1487=
XM_011539849.1:c.5383G= XP_011538151.1:p.Ala1795=
XM_011539850.1:c.4228G= XP_011538152.1:p.Ala1410=
XM_006717885.4:c.5383G= XP_006717948.1:p.Ala1795=
XM_006717888.4:c.5380G= XP_006717951.1:p.Ala1794=
XM_006717889.4:c.5335G= XP_006717952.1:p.Ala1779=
XM_006717890.3:c.4459G= XP_006717953.1:p.Ala1487=
XM_011539849.3:c.5383G= XP_011538151.1:p.Ala1795=
XM_011539850.3:c.4228G= XP_011538152.1:p.Ala1410=
XM_017016310.2:c.5383G= XP_016871799.1:p.Ala1795=
XM_017016311.2:c.5383G= XP_016871800.1:p.Ala1795=
XM_017016312.2:c.4369G= XP_016871801.1:p.Ala1457=
NM_001288989.2:c.5293G= NP_001275918.1:p.Ala1765=
NM_016341.4:c.5341G= MANE Select NP_057425.3:p.Ala1781=