Canonical Allele Identifier: CA377642023
Gene: PLCE1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94298553C>G , CM000672.2:g.94298553C>G GRCh38
NC_000010.10:g.96058310C>G , CM000672.1:g.96058310C>G GRCh37
NC_000010.9:g.96048300C>G NCBI36
NG_015799.1:g.309565C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371375.2:c.4418C>G ENSP00000360426.1:p.Ala1473Gly
ENST00000685253.1:c.*1885C>G ENSP00000509405.1:n.*1885C>G
ENST00000685889.1:n.2077C>G
ENST00000686807.1:n.761C>G
ENST00000686954.1:c.*626C>G ENSP00000508416.1:n.*626C>G
ENST00000688810.1:c.4370C>G ENSP00000509140.1:p.Ala1457Gly
ENST00000689233.1:n.9550C>G
ENST00000690340.1:n.3015C>G
ENST00000692286.1:c.5210C>G ENSP00000509490.1:p.Ala1737Gly
ENST00000692396.1:c.5294C>G ENSP00000508605.1:p.Ala1765Gly
ENST00000371380.8:c.5342C>G MANE Select ENSP00000360431.2:p.Ala1781Gly
ENST00000371385.8:c.4316C>G ENSP00000360438.4:p.Ala1439Gly
ENST00000674738.1:c.3897C>G
ENST00000674827.1:c.3458C>G ENSP00000502523.1:p.Ala1153Gly
ENST00000675218.1:c.4418C>G ENSP00000501910.1:p.Ala1473Gly
ENST00000675487.1:c.*1275C>G ENSP00000502340.1:n.*1275C>G
ENST00000675718.1:c.4611C>G
ENST00000260766.7:c.5342C>G ENSP00000260766.3:p.Ala1781Gly
ENST00000371375.1:c.4418C>G ENSP00000360426.1:p.Ala1473Gly
ENST00000371380.7:c.5342C>G ENSP00000360431.2:p.Ala1781Gly
ENST00000371385.7:c.4418C>G ENSP00000360438.3:p.Ala1473Gly
NM_001165979.2:c.4418C>G NP_001159451.1:p.Ala1473Gly
NM_001288989.1:c.5294C>G NP_001275918.1:p.Ala1765Gly
NM_016341.3:c.5342C>G NP_057425.3:p.Ala1781Gly
XM_006717885.2:c.5384C>G XP_006717948.1:p.Ala1795Gly
XM_006717886.2:c.5384C>G XP_006717949.1:p.Ala1795Gly
XM_006717888.2:c.5381C>G XP_006717951.1:p.Ala1794Gly
XM_006717889.2:c.5336C>G XP_006717952.1:p.Ala1779Gly
XM_006717890.1:c.4460C>G XP_006717953.1:p.Ala1487Gly
XM_011539849.1:c.5384C>G XP_011538151.1:p.Ala1795Gly
XM_011539850.1:c.4229C>G XP_011538152.1:p.Ala1410Gly
XM_006717885.4:c.5384C>G XP_006717948.1:p.Ala1795Gly
XM_006717888.4:c.5381C>G XP_006717951.1:p.Ala1794Gly
XM_006717889.4:c.5336C>G XP_006717952.1:p.Ala1779Gly
XM_006717890.3:c.4460C>G XP_006717953.1:p.Ala1487Gly
XM_011539849.3:c.5384C>G XP_011538151.1:p.Ala1795Gly
XM_011539850.3:c.4229C>G XP_011538152.1:p.Ala1410Gly
XM_017016310.2:c.5384C>G XP_016871799.1:p.Ala1795Gly
XM_017016311.2:c.5384C>G XP_016871800.1:p.Ala1795Gly
XM_017016312.2:c.4370C>G XP_016871801.1:p.Ala1457Gly
NM_001288989.2:c.5294C>G NP_001275918.1:p.Ala1765Gly
NM_016341.4:c.5342C>G MANE Select NP_057425.3:p.Ala1781Gly