Canonical Allele Identifier: CA377640545

Gene: PLCE1

Linked Data

• MyVariant Identifiers: chr10:g.96053299A>T (hg19) ; chr10:g.94293542A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94293542A>T , CM000672.2:g.94293542A>T	GRCh38
NC_000010.10:g.96053299A>T , CM000672.1:g.96053299A>T	GRCh37
NC_000010.9:g.96043289A>T	NCBI36
NG_015799.1:g.304554A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371375.2:c.4146A>T	ENSP00000360426.1:p.Arg1382Ser
ENST00000685253.1:c.*1613A>T	ENSP00000509405.1:n.*1613A>T
ENST00000685889.1:n.1805A>T
ENST00000686807.1:n.489A>T
ENST00000686954.1:c.*354A>T	ENSP00000508416.1:n.*354A>T
ENST00000688810.1:c.4098A>T	ENSP00000509140.1:p.Arg1366Ser
ENST00000689233.1:n.9278A>T
ENST00000690340.1:n.2743A>T
ENST00000692286.1:c.5036-4837A>T	ENSP00000509490.1:n.5036-4837A>T
ENST00000692396.1:c.5022A>T	ENSP00000508605.1:p.Arg1674Ser
ENST00000371380.8:c.5070A>T MANE Select	ENSP00000360431.2:p.Arg1690Ser
ENST00000371385.8:c.4044A>T	ENSP00000360438.4:p.Arg1348Ser
ENST00000674738.1:c.3625A>T
ENST00000674827.1:c.3186A>T	ENSP00000502523.1:p.Arg1062Ser
ENST00000675218.1:c.4146A>T	ENSP00000501910.1:p.Arg1382Ser
ENST00000675487.1:c.*1003A>T	ENSP00000502340.1:n.*1003A>T
ENST00000675718.1:c.4339A>T
ENST00000676102.1:c.3915A>T	ENSP00000502811.1:p.Arg1305Ser
ENST00000260766.7:c.5070A>T	ENSP00000260766.3:p.Arg1690Ser
ENST00000371375.1:c.4146A>T	ENSP00000360426.1:p.Arg1382Ser
ENST00000371380.7:c.5070A>T	ENSP00000360431.2:p.Arg1690Ser
ENST00000371385.7:c.4146A>T	ENSP00000360438.3:p.Arg1382Ser
NM_001165979.2:c.4146A>T	NP_001159451.1:p.Arg1382Ser
NM_001288989.1:c.5022A>T	NP_001275918.1:p.Arg1674Ser
NM_016341.3:c.5070A>T	NP_057425.3:p.Arg1690Ser
XM_006717885.2:c.5112A>T	XP_006717948.1:p.Arg1704Ser
XM_006717886.2:c.5112A>T	XP_006717949.1:p.Arg1704Ser
XM_006717888.2:c.5109A>T	XP_006717951.1:p.Arg1703Ser
XM_006717889.2:c.5064A>T	XP_006717952.1:p.Arg1688Ser
XM_006717890.1:c.4188A>T	XP_006717953.1:p.Arg1396Ser
XM_011539849.1:c.5112A>T	XP_011538151.1:p.Arg1704Ser
XM_011539850.1:c.3957A>T	XP_011538152.1:p.Arg1319Ser
XM_006717885.4:c.5112A>T	XP_006717948.1:p.Arg1704Ser
XM_006717888.4:c.5109A>T	XP_006717951.1:p.Arg1703Ser
XM_006717889.4:c.5064A>T	XP_006717952.1:p.Arg1688Ser
XM_006717890.3:c.4188A>T	XP_006717953.1:p.Arg1396Ser
XM_011539849.3:c.5112A>T	XP_011538151.1:p.Arg1704Ser
XM_011539850.3:c.3957A>T	XP_011538152.1:p.Arg1319Ser
XM_017016310.2:c.5112A>T	XP_016871799.1:p.Arg1704Ser
XM_017016311.2:c.5112A>T	XP_016871800.1:p.Arg1704Ser
XM_017016312.2:c.4098A>T	XP_016871801.1:p.Arg1366Ser
NM_001288989.2:c.5022A>T	NP_001275918.1:p.Arg1674Ser
NM_016341.4:c.5070A>T MANE Select	NP_057425.3:p.Arg1690Ser