Canonical Allele Identifier: CA377641680
Gene: PLCE1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94298391G>T , CM000672.2:g.94298391G>T GRCh38
NC_000010.10:g.96058148G>T , CM000672.1:g.96058148G>T GRCh37
NC_000010.9:g.96048138G>T NCBI36
NG_015799.1:g.309403G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371375.2:c.4256G>T ENSP00000360426.1:p.Gly1419Val
ENST00000685253.1:c.*1723G>T ENSP00000509405.1:n.*1723G>T
ENST00000685889.1:n.1915G>T
ENST00000686807.1:n.599G>T
ENST00000686954.1:c.*464G>T ENSP00000508416.1:n.*464G>T
ENST00000688810.1:c.4208G>T ENSP00000509140.1:p.Gly1403Val
ENST00000689233.1:n.9388G>T
ENST00000690340.1:n.2853G>T
ENST00000692286.1:c.5048G>T ENSP00000509490.1:p.Gly1683Val
ENST00000692396.1:c.5132G>T ENSP00000508605.1:p.Gly1711Val
ENST00000371380.8:c.5180G>T MANE Select ENSP00000360431.2:p.Gly1727Val
ENST00000371385.8:c.4154G>T ENSP00000360438.4:p.Gly1385Val
ENST00000674738.1:c.3735G>T
ENST00000674827.1:c.3296G>T ENSP00000502523.1:p.Gly1099Val
ENST00000675218.1:c.4256G>T ENSP00000501910.1:p.Gly1419Val
ENST00000675487.1:c.*1113G>T ENSP00000502340.1:n.*1113G>T
ENST00000675718.1:c.4449G>T
ENST00000676102.1:c.4025G>T ENSP00000502811.1:p.Gly1342Val
ENST00000260766.7:c.5180G>T ENSP00000260766.3:p.Gly1727Val
ENST00000371375.1:c.4256G>T ENSP00000360426.1:p.Gly1419Val
ENST00000371380.7:c.5180G>T ENSP00000360431.2:p.Gly1727Val
ENST00000371385.7:c.4256G>T ENSP00000360438.3:p.Gly1419Val
NM_001165979.2:c.4256G>T NP_001159451.1:p.Gly1419Val
NM_001288989.1:c.5132G>T NP_001275918.1:p.Gly1711Val
NM_016341.3:c.5180G>T NP_057425.3:p.Gly1727Val
XM_006717885.2:c.5222G>T XP_006717948.1:p.Gly1741Val
XM_006717886.2:c.5222G>T XP_006717949.1:p.Gly1741Val
XM_006717888.2:c.5219G>T XP_006717951.1:p.Gly1740Val
XM_006717889.2:c.5174G>T XP_006717952.1:p.Gly1725Val
XM_006717890.1:c.4298G>T XP_006717953.1:p.Gly1433Val
XM_011539849.1:c.5222G>T XP_011538151.1:p.Gly1741Val
XM_011539850.1:c.4067G>T XP_011538152.1:p.Gly1356Val
XM_006717885.4:c.5222G>T XP_006717948.1:p.Gly1741Val
XM_006717888.4:c.5219G>T XP_006717951.1:p.Gly1740Val
XM_006717889.4:c.5174G>T XP_006717952.1:p.Gly1725Val
XM_006717890.3:c.4298G>T XP_006717953.1:p.Gly1433Val
XM_011539849.3:c.5222G>T XP_011538151.1:p.Gly1741Val
XM_011539850.3:c.4067G>T XP_011538152.1:p.Gly1356Val
XM_017016310.2:c.5222G>T XP_016871799.1:p.Gly1741Val
XM_017016311.2:c.5222G>T XP_016871800.1:p.Gly1741Val
XM_017016312.2:c.4208G>T XP_016871801.1:p.Gly1403Val
NM_001288989.2:c.5132G>T NP_001275918.1:p.Gly1711Val
NM_016341.4:c.5180G>T MANE Select NP_057425.3:p.Gly1727Val