Canonical Allele Identifier: CA377640553

Gene: PLCE1

Linked Data

• MyVariant Identifiers: chr10:g.96053301G>A (hg19) ; chr10:g.94293544G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94293544G>A , CM000672.2:g.94293544G>A	GRCh38
NC_000010.10:g.96053301G>A , CM000672.1:g.96053301G>A	GRCh37
NC_000010.9:g.96043291G>A	NCBI36
NG_015799.1:g.304556G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.4148G>A	ENSP00000360426.1:p.Gly1383Glu
ENST00000685253.1:c.*1615G>A	ENSP00000509405.1:n.*1615G>A
ENST00000685889.1:n.1807G>A
ENST00000686807.1:n.491G>A
ENST00000686954.1:c.*356G>A	ENSP00000508416.1:n.*356G>A
ENST00000688810.1:c.4100G>A	ENSP00000509140.1:p.Gly1367Glu
ENST00000689233.1:n.9280G>A
ENST00000690340.1:n.2745G>A
ENST00000692286.1:c.5036-4835G>A	ENSP00000509490.1:n.5036-4835G>A
ENST00000692396.1:c.5024G>A	ENSP00000508605.1:p.Gly1675Glu
ENST00000371380.8:c.5072G>A MANE Select	ENSP00000360431.2:p.Gly1691Glu
ENST00000371385.8:c.4046G>A	ENSP00000360438.4:p.Gly1349Glu
ENST00000674738.1:c.3627G>A
ENST00000674827.1:c.3188G>A	ENSP00000502523.1:p.Gly1063Glu
ENST00000675218.1:c.4148G>A	ENSP00000501910.1:p.Gly1383Glu
ENST00000675487.1:c.*1005G>A	ENSP00000502340.1:n.*1005G>A
ENST00000675718.1:c.4341G>A
ENST00000676102.1:c.3917G>A	ENSP00000502811.1:p.Gly1306Glu
ENST00000260766.7:c.5072G>A	ENSP00000260766.3:p.Gly1691Glu
ENST00000371375.1:c.4148G>A	ENSP00000360426.1:p.Gly1383Glu
ENST00000371380.7:c.5072G>A	ENSP00000360431.2:p.Gly1691Glu
ENST00000371385.7:c.4148G>A	ENSP00000360438.3:p.Gly1383Glu
NM_001165979.2:c.4148G>A	NP_001159451.1:p.Gly1383Glu
NM_001288989.1:c.5024G>A	NP_001275918.1:p.Gly1675Glu
NM_016341.3:c.5072G>A	NP_057425.3:p.Gly1691Glu
XM_006717885.2:c.5114G>A	XP_006717948.1:p.Gly1705Glu
XM_006717886.2:c.5114G>A	XP_006717949.1:p.Gly1705Glu
XM_006717888.2:c.5111G>A	XP_006717951.1:p.Gly1704Glu
XM_006717889.2:c.5066G>A	XP_006717952.1:p.Gly1689Glu
XM_006717890.1:c.4190G>A	XP_006717953.1:p.Gly1397Glu
XM_011539849.1:c.5114G>A	XP_011538151.1:p.Gly1705Glu
XM_011539850.1:c.3959G>A	XP_011538152.1:p.Gly1320Glu
XM_006717885.4:c.5114G>A	XP_006717948.1:p.Gly1705Glu
XM_006717888.4:c.5111G>A	XP_006717951.1:p.Gly1704Glu
XM_006717889.4:c.5066G>A	XP_006717952.1:p.Gly1689Glu
XM_006717890.3:c.4190G>A	XP_006717953.1:p.Gly1397Glu
XM_011539849.3:c.5114G>A	XP_011538151.1:p.Gly1705Glu
XM_011539850.3:c.3959G>A	XP_011538152.1:p.Gly1320Glu
XM_017016310.2:c.5114G>A	XP_016871799.1:p.Gly1705Glu
XM_017016311.2:c.5114G>A	XP_016871800.1:p.Gly1705Glu
XM_017016312.2:c.4100G>A	XP_016871801.1:p.Gly1367Glu
NM_001288989.2:c.5024G>A	NP_001275918.1:p.Gly1675Glu
NM_016341.4:c.5072G>A MANE Select	NP_057425.3:p.Gly1691Glu