Canonical Allele Identifier: CA470986453
Gene: PLCE1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96058200C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94298443C>G , CM000672.2:g.94298443C>G GRCh38
NC_000010.10:g.96058200C>G , CM000672.1:g.96058200C>G GRCh37
NC_000010.9:g.96048190C>G NCBI36
NG_015799.1:g.309455C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371375.2:c.4308C>G ENSP00000360426.1:p.Ser1436=
ENST00000685253.1:c.*1775C>G ENSP00000509405.1:n.*1775C>G
ENST00000685889.1:n.1967C>G
ENST00000686807.1:n.651C>G
ENST00000686954.1:c.*516C>G ENSP00000508416.1:n.*516C>G
ENST00000688810.1:c.4260C>G ENSP00000509140.1:p.Ser1420=
ENST00000689233.1:n.9440C>G
ENST00000690340.1:n.2905C>G
ENST00000692286.1:c.5100C>G ENSP00000509490.1:p.Ser1700=
ENST00000692396.1:c.5184C>G ENSP00000508605.1:p.Ser1728=
ENST00000371380.8:c.5232C>G MANE Select ENSP00000360431.2:p.Ser1744=
ENST00000371385.8:c.4206C>G ENSP00000360438.4:p.Ser1402=
ENST00000674738.1:c.3787C>G
ENST00000674827.1:c.3348C>G ENSP00000502523.1:p.Ser1116=
ENST00000675218.1:c.4308C>G ENSP00000501910.1:p.Ser1436=
ENST00000675487.1:c.*1165C>G ENSP00000502340.1:n.*1165C>G
ENST00000675718.1:c.4501C>G
ENST00000676102.1:c.4077C>G ENSP00000502811.1:p.Ser1359=
ENST00000260766.7:c.5232C>G ENSP00000260766.3:p.Ser1744=
ENST00000371375.1:c.4308C>G ENSP00000360426.1:p.Ser1436=
ENST00000371380.7:c.5232C>G ENSP00000360431.2:p.Ser1744=
ENST00000371385.7:c.4308C>G ENSP00000360438.3:p.Ser1436=
NM_001165979.2:c.4308C>G NP_001159451.1:p.Ser1436=
NM_001288989.1:c.5184C>G NP_001275918.1:p.Ser1728=
NM_016341.3:c.5232C>G NP_057425.3:p.Ser1744=
XM_006717885.2:c.5274C>G XP_006717948.1:p.Ser1758=
XM_006717886.2:c.5274C>G XP_006717949.1:p.Ser1758=
XM_006717888.2:c.5271C>G XP_006717951.1:p.Ser1757=
XM_006717889.2:c.5226C>G XP_006717952.1:p.Ser1742=
XM_006717890.1:c.4350C>G XP_006717953.1:p.Ser1450=
XM_011539849.1:c.5274C>G XP_011538151.1:p.Ser1758=
XM_011539850.1:c.4119C>G XP_011538152.1:p.Ser1373=
XM_006717885.4:c.5274C>G XP_006717948.1:p.Ser1758=
XM_006717888.4:c.5271C>G XP_006717951.1:p.Ser1757=
XM_006717889.4:c.5226C>G XP_006717952.1:p.Ser1742=
XM_006717890.3:c.4350C>G XP_006717953.1:p.Ser1450=
XM_011539849.3:c.5274C>G XP_011538151.1:p.Ser1758=
XM_011539850.3:c.4119C>G XP_011538152.1:p.Ser1373=
XM_017016310.2:c.5274C>G XP_016871799.1:p.Ser1758=
XM_017016311.2:c.5274C>G XP_016871800.1:p.Ser1758=
XM_017016312.2:c.4260C>G XP_016871801.1:p.Ser1420=
NM_001288989.2:c.5184C>G NP_001275918.1:p.Ser1728=
NM_016341.4:c.5232C>G MANE Select NP_057425.3:p.Ser1744=