Canonical Allele Identifier: CA377641801
Gene: PLCE1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94298451C>G , CM000672.2:g.94298451C>G GRCh38
NC_000010.10:g.96058208C>G , CM000672.1:g.96058208C>G GRCh37
NC_000010.9:g.96048198C>G NCBI36
NG_015799.1:g.309463C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371375.2:n.4316C>G ENSP00000360426.1:p.Ala1439Gly
ENST00000685253.1:c.*1783C>G ENSP00000509405.1:n.*1783C>G
ENST00000685889.1:n.1975C>G
ENST00000686807.1:n.659C>G
ENST00000686954.1:c.*524C>G ENSP00000508416.1:n.*524C>G
ENST00000688810.1:n.4268C>G ENSP00000509140.1:p.Ala1423Gly
ENST00000689233.1:n.9448C>G
ENST00000690340.1:n.2913C>G
ENST00000692286.1:c.5108C>G ENSP00000509490.1:p.Ala1703Gly
ENST00000692396.1:c.5192C>G ENSP00000508605.1:p.Ala1731Gly
ENST00000371380.8:c.5240C>G MANE Select ENSP00000360431.2:p.Ala1747Gly
ENST00000371385.8:c.4214C>G ENSP00000360438.4:p.Ala1405Gly
ENST00000674738.1:n.3795C>G
ENST00000674827.1:n.3356C>G ENSP00000502523.1:p.Ala1119Gly
ENST00000675218.1:n.4316C>G ENSP00000501910.1:p.Ala1439Gly
ENST00000675487.1:c.*1173C>G ENSP00000502340.1:n.*1173C>G
ENST00000675718.1:n.4509C>G
ENST00000676102.1:c.4085C>G ENSP00000502811.1:p.Ala1362Gly
ENST00000260766.7:c.5240C>G ENSP00000260766.3:p.Ala1747Gly
ENST00000371375.1:n.4316C>G ENSP00000360426.1:p.Ala1439Gly
ENST00000371380.7:c.5240C>G ENSP00000360431.2:p.Ala1747Gly
ENST00000371385.7:c.4316C>G ENSP00000360438.3:p.Ala1439Gly
NM_001165979.2:c.4316C>G NP_001159451.1:p.Ala1439Gly
NM_001288989.1:c.5192C>G NP_001275918.1:p.Ala1731Gly
NM_016341.3:c.5240C>G NP_057425.3:p.Ala1747Gly
XM_006717885.2:c.5282C>G XP_006717948.1:p.Ala1761Gly
XM_006717886.2:c.5282C>G XP_006717949.1:p.Ala1761Gly
XM_006717888.2:c.5279C>G XP_006717951.1:p.Ala1760Gly
XM_006717889.2:c.5234C>G XP_006717952.1:p.Ala1745Gly
XM_006717890.1:c.4358C>G XP_006717953.1:p.Ala1453Gly
XM_011539849.1:c.5282C>G XP_011538151.1:p.Ala1761Gly
XM_011539850.1:c.4127C>G XP_011538152.1:p.Ala1376Gly
XM_006717885.4:c.5282C>G XP_006717948.1:p.Ala1761Gly
XM_006717888.4:c.5279C>G XP_006717951.1:p.Ala1760Gly
XM_006717889.4:c.5234C>G XP_006717952.1:p.Ala1745Gly
XM_006717890.3:c.4358C>G XP_006717953.1:p.Ala1453Gly
XM_011539849.3:c.5282C>G XP_011538151.1:p.Ala1761Gly
XM_011539850.3:c.4127C>G XP_011538152.1:p.Ala1376Gly
XM_017016310.2:c.5282C>G XP_016871799.1:p.Ala1761Gly
XM_017016311.2:c.5282C>G XP_016871800.1:p.Ala1761Gly
XM_017016312.2:c.4268C>G XP_016871801.1:p.Ala1423Gly
NM_001288989.2:c.5192C>G NP_001275918.1:p.Ala1731Gly
NM_016341.4:c.5240C>G MANE Select NP_057425.3:p.Ala1747Gly