Canonical Allele Identifier: CA470986399

Gene: PLCE1

Linked Data

• gnomAD v4: 10-94298392-C-T
• MyVariant Identifiers: chr10:g.96058149C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298392C>T , CM000672.2:g.94298392C>T	GRCh38
NC_000010.10:g.96058149C>T , CM000672.1:g.96058149C>T	GRCh37
NC_000010.9:g.96048139C>T	NCBI36
NG_015799.1:g.309404C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371375.2:c.4257C>T	ENSP00000360426.1:p.Gly1419=
ENST00000685253.1:c.*1724C>T	ENSP00000509405.1:n.*1724C>T
ENST00000685889.1:n.1916C>T
ENST00000686807.1:n.600C>T
ENST00000686954.1:c.*465C>T	ENSP00000508416.1:n.*465C>T
ENST00000688810.1:c.4209C>T	ENSP00000509140.1:p.Gly1403=
ENST00000689233.1:n.9389C>T
ENST00000690340.1:n.2854C>T
ENST00000692286.1:c.5049C>T	ENSP00000509490.1:p.Gly1683=
ENST00000692396.1:c.5133C>T	ENSP00000508605.1:p.Gly1711=
ENST00000371380.8:c.5181C>T MANE Select	ENSP00000360431.2:p.Gly1727=
ENST00000371385.8:c.4155C>T	ENSP00000360438.4:p.Gly1385=
ENST00000674738.1:c.3736C>T
ENST00000674827.1:c.3297C>T	ENSP00000502523.1:p.Gly1099=
ENST00000675218.1:c.4257C>T	ENSP00000501910.1:p.Gly1419=
ENST00000675487.1:c.*1114C>T	ENSP00000502340.1:n.*1114C>T
ENST00000675718.1:c.4450C>T
ENST00000676102.1:c.4026C>T	ENSP00000502811.1:p.Gly1342=
ENST00000260766.7:c.5181C>T	ENSP00000260766.3:p.Gly1727=
ENST00000371375.1:c.4257C>T	ENSP00000360426.1:p.Gly1419=
ENST00000371380.7:c.5181C>T	ENSP00000360431.2:p.Gly1727=
ENST00000371385.7:c.4257C>T	ENSP00000360438.3:p.Gly1419=
NM_001165979.2:c.4257C>T	NP_001159451.1:p.Gly1419=
NM_001288989.1:c.5133C>T	NP_001275918.1:p.Gly1711=
NM_016341.3:c.5181C>T	NP_057425.3:p.Gly1727=
XM_006717885.2:c.5223C>T	XP_006717948.1:p.Gly1741=
XM_006717886.2:c.5223C>T	XP_006717949.1:p.Gly1741=
XM_006717888.2:c.5220C>T	XP_006717951.1:p.Gly1740=
XM_006717889.2:c.5175C>T	XP_006717952.1:p.Gly1725=
XM_006717890.1:c.4299C>T	XP_006717953.1:p.Gly1433=
XM_011539849.1:c.5223C>T	XP_011538151.1:p.Gly1741=
XM_011539850.1:c.4068C>T	XP_011538152.1:p.Gly1356=
XM_006717885.4:c.5223C>T	XP_006717948.1:p.Gly1741=
XM_006717888.4:c.5220C>T	XP_006717951.1:p.Gly1740=
XM_006717889.4:c.5175C>T	XP_006717952.1:p.Gly1725=
XM_006717890.3:c.4299C>T	XP_006717953.1:p.Gly1433=
XM_011539849.3:c.5223C>T	XP_011538151.1:p.Gly1741=
XM_011539850.3:c.4068C>T	XP_011538152.1:p.Gly1356=
XM_017016310.2:c.5223C>T	XP_016871799.1:p.Gly1741=
XM_017016311.2:c.5223C>T	XP_016871800.1:p.Gly1741=
XM_017016312.2:c.4209C>T	XP_016871801.1:p.Gly1403=
NM_001288989.2:c.5133C>T	NP_001275918.1:p.Gly1711=
NM_016341.4:c.5181C>T MANE Select	NP_057425.3:p.Gly1727=