Canonical Allele Identifier: CA377642258

Gene: PLCE1

Linked Data

• MyVariant Identifiers: chr10:g.96058396C>T (hg19) ; chr10:g.94298639C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298639C>T , CM000672.2:g.94298639C>T	GRCh38
NC_000010.10:g.96058396C>T , CM000672.1:g.96058396C>T	GRCh37
NC_000010.9:g.96048386C>T	NCBI36
NG_015799.1:g.309651C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.4504C>T	ENSP00000360426.1:p.Gln1502Ter
ENST00000685253.1:c.*1971C>T	ENSP00000509405.1:n.*1971C>T
ENST00000685889.1:n.2163C>T
ENST00000686807.1:n.847C>T
ENST00000686954.1:c.*712C>T	ENSP00000508416.1:n.*712C>T
ENST00000688810.1:c.4456C>T	ENSP00000509140.1:p.Gln1486Ter
ENST00000689233.1:n.9636C>T
ENST00000690340.1:n.3101C>T
ENST00000692286.1:c.5296C>T	ENSP00000509490.1:p.Gln1766Ter
ENST00000692396.1:c.5380C>T	ENSP00000508605.1:p.Gln1794Ter
ENST00000371380.8:c.5428C>T MANE Select	ENSP00000360431.2:p.Gln1810Ter
ENST00000371385.8:c.4402C>T	ENSP00000360438.4:p.Gln1468Ter
ENST00000674738.1:c.3983C>T
ENST00000674827.1:c.3544C>T	ENSP00000502523.1:p.Gln1182Ter
ENST00000675218.1:c.4504C>T	ENSP00000501910.1:p.Gln1502Ter
ENST00000675487.1:c.*1361C>T	ENSP00000502340.1:n.*1361C>T
ENST00000675718.1:c.4697C>T
ENST00000260766.7:c.5428C>T	ENSP00000260766.3:p.Gln1810Ter
ENST00000371375.1:c.4504C>T	ENSP00000360426.1:p.Gln1502Ter
ENST00000371380.7:c.5428C>T	ENSP00000360431.2:p.Gln1810Ter
ENST00000371385.7:c.4504C>T	ENSP00000360438.3:p.Gln1502Ter
NM_001165979.2:c.4504C>T	NP_001159451.1:p.Gln1502Ter
NM_001288989.1:c.5380C>T	NP_001275918.1:p.Gln1794Ter
NM_016341.3:c.5428C>T	NP_057425.3:p.Gln1810Ter
XM_006717885.2:c.5470C>T	XP_006717948.1:p.Gln1824Ter
XM_006717886.2:c.5470C>T	XP_006717949.1:p.Gln1824Ter
XM_006717888.2:c.5467C>T	XP_006717951.1:p.Gln1823Ter
XM_006717889.2:c.5422C>T	XP_006717952.1:p.Gln1808Ter
XM_006717890.1:c.4546C>T	XP_006717953.1:p.Gln1516Ter
XM_011539849.1:c.5470C>T	XP_011538151.1:p.Gln1824Ter
XM_011539850.1:c.4315C>T	XP_011538152.1:p.Gln1439Ter
XM_006717885.4:c.5470C>T	XP_006717948.1:p.Gln1824Ter
XM_006717888.4:c.5467C>T	XP_006717951.1:p.Gln1823Ter
XM_006717889.4:c.5422C>T	XP_006717952.1:p.Gln1808Ter
XM_006717890.3:c.4546C>T	XP_006717953.1:p.Gln1516Ter
XM_011539849.3:c.5470C>T	XP_011538151.1:p.Gln1824Ter
XM_011539850.3:c.4315C>T	XP_011538152.1:p.Gln1439Ter
XM_017016310.2:c.5470C>T	XP_016871799.1:p.Gln1824Ter
XM_017016311.2:c.5470C>T	XP_016871800.1:p.Gln1824Ter
XM_017016312.2:c.4456C>T	XP_016871801.1:p.Gln1486Ter
NM_001288989.2:c.5380C>T	NP_001275918.1:p.Gln1794Ter
NM_016341.4:c.5428C>T MANE Select	NP_057425.3:p.Gln1810Ter