Canonical Allele Identifier: CA377642289

Gene: PLCE1

Linked Data

• MyVariant Identifiers: chr10:g.96058403T>A (hg19) ; chr10:g.94298646T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298646T>A , CM000672.2:g.94298646T>A	GRCh38
NC_000010.10:g.96058403T>A , CM000672.1:g.96058403T>A	GRCh37
NC_000010.9:g.96048393T>A	NCBI36
NG_015799.1:g.309658T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.4511T>A	ENSP00000360426.1:p.Val1504Glu
ENST00000685253.1:c.*1978T>A	ENSP00000509405.1:n.*1978T>A
ENST00000685889.1:n.2170T>A
ENST00000686807.1:n.854T>A
ENST00000686954.1:c.*719T>A	ENSP00000508416.1:n.*719T>A
ENST00000688810.1:c.4463T>A	ENSP00000509140.1:p.Val1488Glu
ENST00000689233.1:n.9643T>A
ENST00000690340.1:n.3108T>A
ENST00000692286.1:c.5303T>A	ENSP00000509490.1:p.Val1768Glu
ENST00000692396.1:c.5387T>A	ENSP00000508605.1:p.Val1796Glu
ENST00000371380.8:c.5435T>A MANE Select	ENSP00000360431.2:p.Val1812Glu
ENST00000371385.8:c.4409T>A	ENSP00000360438.4:p.Val1470Glu
ENST00000674738.1:c.3990T>A
ENST00000674827.1:c.3551T>A	ENSP00000502523.1:p.Val1184Glu
ENST00000675218.1:c.4511T>A	ENSP00000501910.1:p.Val1504Glu
ENST00000675487.1:c.*1368T>A	ENSP00000502340.1:n.*1368T>A
ENST00000675718.1:c.4704T>A
ENST00000260766.7:c.5435T>A	ENSP00000260766.3:p.Val1812Glu
ENST00000371375.1:c.4511T>A	ENSP00000360426.1:p.Val1504Glu
ENST00000371380.7:c.5435T>A	ENSP00000360431.2:p.Val1812Glu
ENST00000371385.7:c.4511T>A	ENSP00000360438.3:p.Val1504Glu
NM_001165979.2:c.4511T>A	NP_001159451.1:p.Val1504Glu
NM_001288989.1:c.5387T>A	NP_001275918.1:p.Val1796Glu
NM_016341.3:c.5435T>A	NP_057425.3:p.Val1812Glu
XM_006717885.2:c.5477T>A	XP_006717948.1:p.Val1826Glu
XM_006717886.2:c.5477T>A	XP_006717949.1:p.Val1826Glu
XM_006717888.2:c.5474T>A	XP_006717951.1:p.Val1825Glu
XM_006717889.2:c.5429T>A	XP_006717952.1:p.Val1810Glu
XM_006717890.1:c.4553T>A	XP_006717953.1:p.Val1518Glu
XM_011539849.1:c.5477T>A	XP_011538151.1:p.Val1826Glu
XM_011539850.1:c.4322T>A	XP_011538152.1:p.Val1441Glu
XM_006717885.4:c.5477T>A	XP_006717948.1:p.Val1826Glu
XM_006717888.4:c.5474T>A	XP_006717951.1:p.Val1825Glu
XM_006717889.4:c.5429T>A	XP_006717952.1:p.Val1810Glu
XM_006717890.3:c.4553T>A	XP_006717953.1:p.Val1518Glu
XM_011539849.3:c.5477T>A	XP_011538151.1:p.Val1826Glu
XM_011539850.3:c.4322T>A	XP_011538152.1:p.Val1441Glu
XM_017016310.2:c.5477T>A	XP_016871799.1:p.Val1826Glu
XM_017016311.2:c.5477T>A	XP_016871800.1:p.Val1826Glu
XM_017016312.2:c.4463T>A	XP_016871801.1:p.Val1488Glu
NM_001288989.2:c.5387T>A	NP_001275918.1:p.Val1796Glu
NM_016341.4:c.5435T>A MANE Select	NP_057425.3:p.Val1812Glu