Canonical Allele Identifier: CA377641700
Gene: PLCE1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94298402A>T , CM000672.2:g.94298402A>T GRCh38
NC_000010.10:g.96058159A>T , CM000672.1:g.96058159A>T GRCh37
NC_000010.9:g.96048149A>T NCBI36
NG_015799.1:g.309414A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371375.2:c.4267A>T ENSP00000360426.1:p.Thr1423Ser
ENST00000685253.1:c.*1734A>T ENSP00000509405.1:n.*1734A>T
ENST00000685889.1:n.1926A>T
ENST00000686807.1:n.610A>T
ENST00000686954.1:c.*475A>T ENSP00000508416.1:n.*475A>T
ENST00000688810.1:c.4219A>T ENSP00000509140.1:p.Thr1407Ser
ENST00000689233.1:n.9399A>T
ENST00000690340.1:n.2864A>T
ENST00000692286.1:c.5059A>T ENSP00000509490.1:p.Thr1687Ser
ENST00000692396.1:c.5143A>T ENSP00000508605.1:p.Thr1715Ser
ENST00000371380.8:c.5191A>T MANE Select ENSP00000360431.2:p.Thr1731Ser
ENST00000371385.8:c.4165A>T ENSP00000360438.4:p.Thr1389Ser
ENST00000674738.1:c.3746A>T
ENST00000674827.1:c.3307A>T ENSP00000502523.1:p.Thr1103Ser
ENST00000675218.1:c.4267A>T ENSP00000501910.1:p.Thr1423Ser
ENST00000675487.1:c.*1124A>T ENSP00000502340.1:n.*1124A>T
ENST00000675718.1:c.4460A>T
ENST00000676102.1:c.4036A>T ENSP00000502811.1:p.Thr1346Ser
ENST00000260766.7:c.5191A>T ENSP00000260766.3:p.Thr1731Ser
ENST00000371375.1:c.4267A>T ENSP00000360426.1:p.Thr1423Ser
ENST00000371380.7:c.5191A>T ENSP00000360431.2:p.Thr1731Ser
ENST00000371385.7:c.4267A>T ENSP00000360438.3:p.Thr1423Ser
NM_001165979.2:c.4267A>T NP_001159451.1:p.Thr1423Ser
NM_001288989.1:c.5143A>T NP_001275918.1:p.Thr1715Ser
NM_016341.3:c.5191A>T NP_057425.3:p.Thr1731Ser
XM_006717885.2:c.5233A>T XP_006717948.1:p.Thr1745Ser
XM_006717886.2:c.5233A>T XP_006717949.1:p.Thr1745Ser
XM_006717888.2:c.5230A>T XP_006717951.1:p.Thr1744Ser
XM_006717889.2:c.5185A>T XP_006717952.1:p.Thr1729Ser
XM_006717890.1:c.4309A>T XP_006717953.1:p.Thr1437Ser
XM_011539849.1:c.5233A>T XP_011538151.1:p.Thr1745Ser
XM_011539850.1:c.4078A>T XP_011538152.1:p.Thr1360Ser
XM_006717885.4:c.5233A>T XP_006717948.1:p.Thr1745Ser
XM_006717888.4:c.5230A>T XP_006717951.1:p.Thr1744Ser
XM_006717889.4:c.5185A>T XP_006717952.1:p.Thr1729Ser
XM_006717890.3:c.4309A>T XP_006717953.1:p.Thr1437Ser
XM_011539849.3:c.5233A>T XP_011538151.1:p.Thr1745Ser
XM_011539850.3:c.4078A>T XP_011538152.1:p.Thr1360Ser
XM_017016310.2:c.5233A>T XP_016871799.1:p.Thr1745Ser
XM_017016311.2:c.5233A>T XP_016871800.1:p.Thr1745Ser
XM_017016312.2:c.4219A>T XP_016871801.1:p.Thr1407Ser
NM_001288989.2:c.5143A>T NP_001275918.1:p.Thr1715Ser
NM_016341.4:c.5191A>T MANE Select NP_057425.3:p.Thr1731Ser