Canonical Allele Identifier: CA1928998400
Gene: PLCE1 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000371375.2:c.4316C= ENSP00000360426.1:p.Ala1439=
ENST00000685253.1:c.*1783C= ENSP00000509405.1:n.*1783C=
ENST00000685889.1:n.1975C=
ENST00000686807.1:n.659C=
ENST00000686954.1:c.*524C= ENSP00000508416.1:n.*524C=
ENST00000688810.1:c.4268C= ENSP00000509140.1:p.Ala1423=
ENST00000689233.1:n.9448C=
ENST00000690340.1:n.2913C=
ENST00000692286.1:c.5108C= ENSP00000509490.1:p.Ala1703=
ENST00000692396.1:c.5192C= ENSP00000508605.1:p.Ala1731=
ENST00000371380.8:c.5240C= MANE Select ENSP00000360431.2:p.Ala1747=
ENST00000371385.8:c.4214C= ENSP00000360438.4:p.Ala1405=
ENST00000674738.1:c.3795C=
ENST00000674827.1:c.3356C= ENSP00000502523.1:p.Ala1119=
ENST00000675218.1:c.4316C= ENSP00000501910.1:p.Ala1439=
ENST00000675487.1:c.*1173C= ENSP00000502340.1:n.*1173C=
ENST00000675718.1:c.4509C=
ENST00000676102.1:c.4085C= ENSP00000502811.1:p.Ala1362=
ENST00000260766.7:c.5240C= ENSP00000260766.3:p.Ala1747=
ENST00000371375.1:c.4316C= ENSP00000360426.1:p.Ala1439=
ENST00000371380.7:c.5240C= ENSP00000360431.2:p.Ala1747=
ENST00000371385.7:c.4316C= ENSP00000360438.3:p.Ala1439=
NM_001165979.2:c.4316C= NP_001159451.1:p.Ala1439=
NM_001288989.1:c.5192C= NP_001275918.1:p.Ala1731=
NM_016341.3:c.5240C= NP_057425.3:p.Ala1747=
XM_006717885.2:c.5282C= XP_006717948.1:p.Ala1761=
XM_006717886.2:c.5282C= XP_006717949.1:p.Ala1761=
XM_006717888.2:c.5279C= XP_006717951.1:p.Ala1760=
XM_006717889.2:c.5234C= XP_006717952.1:p.Ala1745=
XM_006717890.1:c.4358C= XP_006717953.1:p.Ala1453=
XM_011539849.1:c.5282C= XP_011538151.1:p.Ala1761=
XM_011539850.1:c.4127C= XP_011538152.1:p.Ala1376=
XM_006717885.4:c.5282C= XP_006717948.1:p.Ala1761=
XM_006717888.4:c.5279C= XP_006717951.1:p.Ala1760=
XM_006717889.4:c.5234C= XP_006717952.1:p.Ala1745=
XM_006717890.3:c.4358C= XP_006717953.1:p.Ala1453=
XM_011539849.3:c.5282C= XP_011538151.1:p.Ala1761=
XM_011539850.3:c.4127C= XP_011538152.1:p.Ala1376=
XM_017016310.2:c.5282C= XP_016871799.1:p.Ala1761=
XM_017016311.2:c.5282C= XP_016871800.1:p.Ala1761=
XM_017016312.2:c.4268C= XP_016871801.1:p.Ala1423=
NM_001288989.2:c.5192C= NP_001275918.1:p.Ala1731=
NM_016341.4:c.5240C= MANE Select NP_057425.3:p.Ala1747=