Canonical Allele Identifier: CA377642002

Gene: PLCE1

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298543C>T , CM000672.2:g.94298543C>T	GRCh38
NC_000010.10:g.96058300C>T , CM000672.1:g.96058300C>T	GRCh37
NC_000010.9:g.96048290C>T	NCBI36
NG_015799.1:g.309555C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.4408C>T	ENSP00000360426.1:p.Gln1470Ter
ENST00000685253.1:c.*1875C>T	ENSP00000509405.1:n.*1875C>T
ENST00000685889.1:n.2067C>T
ENST00000686807.1:n.751C>T
ENST00000686954.1:c.*616C>T	ENSP00000508416.1:n.*616C>T
ENST00000688810.1:c.4360C>T	ENSP00000509140.1:p.Gln1454Ter
ENST00000689233.1:n.9540C>T
ENST00000690340.1:n.3005C>T
ENST00000692286.1:c.5200C>T	ENSP00000509490.1:p.Gln1734Ter
ENST00000692396.1:c.5284C>T	ENSP00000508605.1:p.Gln1762Ter
ENST00000371380.8:c.5332C>T MANE Select	ENSP00000360431.2:p.Gln1778Ter
ENST00000371385.8:c.4306C>T	ENSP00000360438.4:p.Gln1436Ter
ENST00000674738.1:c.3887C>T
ENST00000674827.1:c.3448C>T	ENSP00000502523.1:p.Gln1150Ter
ENST00000675218.1:c.4408C>T	ENSP00000501910.1:p.Gln1470Ter
ENST00000675487.1:c.*1265C>T	ENSP00000502340.1:n.*1265C>T
ENST00000675718.1:c.4601C>T
ENST00000260766.7:c.5332C>T	ENSP00000260766.3:p.Gln1778Ter
ENST00000371375.1:c.4408C>T	ENSP00000360426.1:p.Gln1470Ter
ENST00000371380.7:c.5332C>T	ENSP00000360431.2:p.Gln1778Ter
ENST00000371385.7:c.4408C>T	ENSP00000360438.3:p.Gln1470Ter
NM_001165979.2:c.4408C>T	NP_001159451.1:p.Gln1470Ter
NM_001288989.1:c.5284C>T	NP_001275918.1:p.Gln1762Ter
NM_016341.3:c.5332C>T	NP_057425.3:p.Gln1778Ter
XM_006717885.2:c.5374C>T	XP_006717948.1:p.Gln1792Ter
XM_006717886.2:c.5374C>T	XP_006717949.1:p.Gln1792Ter
XM_006717888.2:c.5371C>T	XP_006717951.1:p.Gln1791Ter
XM_006717889.2:c.5326C>T	XP_006717952.1:p.Gln1776Ter
XM_006717890.1:c.4450C>T	XP_006717953.1:p.Gln1484Ter
XM_011539849.1:c.5374C>T	XP_011538151.1:p.Gln1792Ter
XM_011539850.1:c.4219C>T	XP_011538152.1:p.Gln1407Ter
XM_006717885.4:c.5374C>T	XP_006717948.1:p.Gln1792Ter
XM_006717888.4:c.5371C>T	XP_006717951.1:p.Gln1791Ter
XM_006717889.4:c.5326C>T	XP_006717952.1:p.Gln1776Ter
XM_006717890.3:c.4450C>T	XP_006717953.1:p.Gln1484Ter
XM_011539849.3:c.5374C>T	XP_011538151.1:p.Gln1792Ter
XM_011539850.3:c.4219C>T	XP_011538152.1:p.Gln1407Ter
XM_017016310.2:c.5374C>T	XP_016871799.1:p.Gln1792Ter
XM_017016311.2:c.5374C>T	XP_016871800.1:p.Gln1792Ter
XM_017016312.2:c.4360C>T	XP_016871801.1:p.Gln1454Ter
NM_001288989.2:c.5284C>T	NP_001275918.1:p.Gln1762Ter
NM_016341.4:c.5332C>T MANE Select	NP_057425.3:p.Gln1778Ter