Canonical Allele Identifier: CA377640707

Gene: PLCE1

Linked Data

• MyVariant Identifiers: chr10:g.96053334G>A (hg19) ; chr10:g.94293577G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94293577G>A , CM000672.2:g.94293577G>A	GRCh38
NC_000010.10:g.96053334G>A , CM000672.1:g.96053334G>A	GRCh37
NC_000010.9:g.96043324G>A	NCBI36
NG_015799.1:g.304589G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.4181G>A	ENSP00000360426.1:p.Gly1394Asp
ENST00000685253.1:c.*1648G>A	ENSP00000509405.1:n.*1648G>A
ENST00000685889.1:n.1840G>A
ENST00000686807.1:n.524G>A
ENST00000686954.1:c.*389G>A	ENSP00000508416.1:n.*389G>A
ENST00000688810.1:c.4133G>A	ENSP00000509140.1:p.Gly1378Asp
ENST00000689233.1:n.9313G>A
ENST00000690340.1:n.2778G>A
ENST00000692286.1:c.5036-4802G>A	ENSP00000509490.1:n.5036-4802G>A
ENST00000692396.1:c.5057G>A	ENSP00000508605.1:p.Gly1686Asp
ENST00000371380.8:c.5105G>A MANE Select	ENSP00000360431.2:p.Gly1702Asp
ENST00000371385.8:c.4079G>A	ENSP00000360438.4:p.Gly1360Asp
ENST00000674738.1:c.3660G>A
ENST00000674827.1:c.3221G>A	ENSP00000502523.1:p.Gly1074Asp
ENST00000675218.1:c.4181G>A	ENSP00000501910.1:p.Gly1394Asp
ENST00000675487.1:c.*1038G>A	ENSP00000502340.1:n.*1038G>A
ENST00000675718.1:c.4374G>A
ENST00000676102.1:c.3950G>A	ENSP00000502811.1:p.Gly1317Asp
ENST00000260766.7:c.5105G>A	ENSP00000260766.3:p.Gly1702Asp
ENST00000371375.1:c.4181G>A	ENSP00000360426.1:p.Gly1394Asp
ENST00000371380.7:c.5105G>A	ENSP00000360431.2:p.Gly1702Asp
ENST00000371385.7:c.4181G>A	ENSP00000360438.3:p.Gly1394Asp
NM_001165979.2:c.4181G>A	NP_001159451.1:p.Gly1394Asp
NM_001288989.1:c.5057G>A	NP_001275918.1:p.Gly1686Asp
NM_016341.3:c.5105G>A	NP_057425.3:p.Gly1702Asp
XM_006717885.2:c.5147G>A	XP_006717948.1:p.Gly1716Asp
XM_006717886.2:c.5147G>A	XP_006717949.1:p.Gly1716Asp
XM_006717888.2:c.5144G>A	XP_006717951.1:p.Gly1715Asp
XM_006717889.2:c.5099G>A	XP_006717952.1:p.Gly1700Asp
XM_006717890.1:c.4223G>A	XP_006717953.1:p.Gly1408Asp
XM_011539849.1:c.5147G>A	XP_011538151.1:p.Gly1716Asp
XM_011539850.1:c.3992G>A	XP_011538152.1:p.Gly1331Asp
XM_006717885.4:c.5147G>A	XP_006717948.1:p.Gly1716Asp
XM_006717888.4:c.5144G>A	XP_006717951.1:p.Gly1715Asp
XM_006717889.4:c.5099G>A	XP_006717952.1:p.Gly1700Asp
XM_006717890.3:c.4223G>A	XP_006717953.1:p.Gly1408Asp
XM_011539849.3:c.5147G>A	XP_011538151.1:p.Gly1716Asp
XM_011539850.3:c.3992G>A	XP_011538152.1:p.Gly1331Asp
XM_017016310.2:c.5147G>A	XP_016871799.1:p.Gly1716Asp
XM_017016311.2:c.5147G>A	XP_016871800.1:p.Gly1716Asp
XM_017016312.2:c.4133G>A	XP_016871801.1:p.Gly1378Asp
NM_001288989.2:c.5057G>A	NP_001275918.1:p.Gly1686Asp
NM_016341.4:c.5105G>A MANE Select	NP_057425.3:p.Gly1702Asp