Canonical Allele Identifier: CA377640667

Gene: PLCE1

Linked Data

• MyVariant Identifiers: chr10:g.96053325C>A (hg19) ; chr10:g.94293568C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94293568C>A , CM000672.2:g.94293568C>A	GRCh38
NC_000010.10:g.96053325C>A , CM000672.1:g.96053325C>A	GRCh37
NC_000010.9:g.96043315C>A	NCBI36
NG_015799.1:g.304580C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000371375.2:c.4172C>A	ENSP00000360426.1:p.Ser1391Tyr
ENST00000685253.1:c.*1639C>A	ENSP00000509405.1:n.*1639C>A
ENST00000685889.1:n.1831C>A
ENST00000686807.1:n.515C>A
ENST00000686954.1:c.*380C>A	ENSP00000508416.1:n.*380C>A
ENST00000688810.1:c.4124C>A	ENSP00000509140.1:p.Ser1375Tyr
ENST00000689233.1:n.9304C>A
ENST00000690340.1:n.2769C>A
ENST00000692286.1:c.5036-4811C>A	ENSP00000509490.1:n.5036-4811C>A
ENST00000692396.1:c.5048C>A	ENSP00000508605.1:p.Ser1683Tyr
ENST00000371380.8:c.5096C>A MANE Select	ENSP00000360431.2:p.Ser1699Tyr
ENST00000371385.8:c.4070C>A	ENSP00000360438.4:p.Ser1357Tyr
ENST00000674738.1:c.3651C>A
ENST00000674827.1:c.3212C>A	ENSP00000502523.1:p.Ser1071Tyr
ENST00000675218.1:c.4172C>A	ENSP00000501910.1:p.Ser1391Tyr
ENST00000675487.1:c.*1029C>A	ENSP00000502340.1:n.*1029C>A
ENST00000675718.1:c.4365C>A
ENST00000676102.1:c.3941C>A	ENSP00000502811.1:p.Ser1314Tyr
ENST00000260766.7:c.5096C>A	ENSP00000260766.3:p.Ser1699Tyr
ENST00000371375.1:c.4172C>A	ENSP00000360426.1:p.Ser1391Tyr
ENST00000371380.7:c.5096C>A	ENSP00000360431.2:p.Ser1699Tyr
ENST00000371385.7:c.4172C>A	ENSP00000360438.3:p.Ser1391Tyr
NM_001165979.2:c.4172C>A	NP_001159451.1:p.Ser1391Tyr
NM_001288989.1:c.5048C>A	NP_001275918.1:p.Ser1683Tyr
NM_016341.3:c.5096C>A	NP_057425.3:p.Ser1699Tyr
XM_006717885.2:c.5138C>A	XP_006717948.1:p.Ser1713Tyr
XM_006717886.2:c.5138C>A	XP_006717949.1:p.Ser1713Tyr
XM_006717888.2:c.5135C>A	XP_006717951.1:p.Ser1712Tyr
XM_006717889.2:c.5090C>A	XP_006717952.1:p.Ser1697Tyr
XM_006717890.1:c.4214C>A	XP_006717953.1:p.Ser1405Tyr
XM_011539849.1:c.5138C>A	XP_011538151.1:p.Ser1713Tyr
XM_011539850.1:c.3983C>A	XP_011538152.1:p.Ser1328Tyr
XM_006717885.4:c.5138C>A	XP_006717948.1:p.Ser1713Tyr
XM_006717888.4:c.5135C>A	XP_006717951.1:p.Ser1712Tyr
XM_006717889.4:c.5090C>A	XP_006717952.1:p.Ser1697Tyr
XM_006717890.3:c.4214C>A	XP_006717953.1:p.Ser1405Tyr
XM_011539849.3:c.5138C>A	XP_011538151.1:p.Ser1713Tyr
XM_011539850.3:c.3983C>A	XP_011538152.1:p.Ser1328Tyr
XM_017016310.2:c.5138C>A	XP_016871799.1:p.Ser1713Tyr
XM_017016311.2:c.5138C>A	XP_016871800.1:p.Ser1713Tyr
XM_017016312.2:c.4124C>A	XP_016871801.1:p.Ser1375Tyr
NM_001288989.2:c.5048C>A	NP_001275918.1:p.Ser1683Tyr
NM_016341.4:c.5096C>A MANE Select	NP_057425.3:p.Ser1699Tyr