Canonical Allele Identifier: CA377642001

Gene: PLCE1

Linked Data

• MyVariant Identifiers: chr10:g.96058300C>G (hg19) ; chr10:g.94298543C>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000371375.2:c.4408C>G	ENSP00000360426.1:p.Gln1470Glu
ENST00000685253.1:c.*1875C>G	ENSP00000509405.1:n.*1875C>G
ENST00000685889.1:n.2067C>G
ENST00000686807.1:n.751C>G
ENST00000686954.1:c.*616C>G	ENSP00000508416.1:n.*616C>G
ENST00000688810.1:c.4360C>G	ENSP00000509140.1:p.Gln1454Glu
ENST00000689233.1:n.9540C>G
ENST00000690340.1:n.3005C>G
ENST00000692286.1:c.5200C>G	ENSP00000509490.1:p.Gln1734Glu
ENST00000692396.1:c.5284C>G	ENSP00000508605.1:p.Gln1762Glu
ENST00000371380.8:c.5332C>G MANE Select	ENSP00000360431.2:p.Gln1778Glu
ENST00000371385.8:c.4306C>G	ENSP00000360438.4:p.Gln1436Glu
ENST00000674738.1:c.3887C>G
ENST00000674827.1:c.3448C>G	ENSP00000502523.1:p.Gln1150Glu
ENST00000675218.1:c.4408C>G	ENSP00000501910.1:p.Gln1470Glu
ENST00000675487.1:c.*1265C>G	ENSP00000502340.1:n.*1265C>G
ENST00000675718.1:c.4601C>G
ENST00000260766.7:c.5332C>G	ENSP00000260766.3:p.Gln1778Glu
ENST00000371375.1:c.4408C>G	ENSP00000360426.1:p.Gln1470Glu
ENST00000371380.7:c.5332C>G	ENSP00000360431.2:p.Gln1778Glu
ENST00000371385.7:c.4408C>G	ENSP00000360438.3:p.Gln1470Glu
NM_001165979.2:c.4408C>G	NP_001159451.1:p.Gln1470Glu
NM_001288989.1:c.5284C>G	NP_001275918.1:p.Gln1762Glu
NM_016341.3:c.5332C>G	NP_057425.3:p.Gln1778Glu
XM_006717885.2:c.5374C>G	XP_006717948.1:p.Gln1792Glu
XM_006717886.2:c.5374C>G	XP_006717949.1:p.Gln1792Glu
XM_006717888.2:c.5371C>G	XP_006717951.1:p.Gln1791Glu
XM_006717889.2:c.5326C>G	XP_006717952.1:p.Gln1776Glu
XM_006717890.1:c.4450C>G	XP_006717953.1:p.Gln1484Glu
XM_011539849.1:c.5374C>G	XP_011538151.1:p.Gln1792Glu
XM_011539850.1:c.4219C>G	XP_011538152.1:p.Gln1407Glu
XM_006717885.4:c.5374C>G	XP_006717948.1:p.Gln1792Glu
XM_006717888.4:c.5371C>G	XP_006717951.1:p.Gln1791Glu
XM_006717889.4:c.5326C>G	XP_006717952.1:p.Gln1776Glu
XM_006717890.3:c.4450C>G	XP_006717953.1:p.Gln1484Glu
XM_011539849.3:c.5374C>G	XP_011538151.1:p.Gln1792Glu
XM_011539850.3:c.4219C>G	XP_011538152.1:p.Gln1407Glu
XM_017016310.2:c.5374C>G	XP_016871799.1:p.Gln1792Glu
XM_017016311.2:c.5374C>G	XP_016871800.1:p.Gln1792Glu
XM_017016312.2:c.4360C>G	XP_016871801.1:p.Gln1454Glu
NM_001288989.2:c.5284C>G	NP_001275918.1:p.Gln1762Glu
NM_016341.4:c.5332C>G MANE Select	NP_057425.3:p.Gln1778Glu