Canonical Allele Identifier: CA377642022

Gene: PLCE1

Linked Data

• MyVariant Identifiers: chr10:g.96058310C>A (hg19) ; chr10:g.94298553C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298553C>A , CM000672.2:g.94298553C>A	GRCh38
NC_000010.10:g.96058310C>A , CM000672.1:g.96058310C>A	GRCh37
NC_000010.9:g.96048300C>A	NCBI36
NG_015799.1:g.309565C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000371375.2:c.4418C>A	ENSP00000360426.1:p.Ala1473Asp
ENST00000685253.1:c.*1885C>A	ENSP00000509405.1:n.*1885C>A
ENST00000685889.1:n.2077C>A
ENST00000686807.1:n.761C>A
ENST00000686954.1:c.*626C>A	ENSP00000508416.1:n.*626C>A
ENST00000688810.1:c.4370C>A	ENSP00000509140.1:p.Ala1457Asp
ENST00000689233.1:n.9550C>A
ENST00000690340.1:n.3015C>A
ENST00000692286.1:c.5210C>A	ENSP00000509490.1:p.Ala1737Asp
ENST00000692396.1:c.5294C>A	ENSP00000508605.1:p.Ala1765Asp
ENST00000371380.8:c.5342C>A MANE Select	ENSP00000360431.2:p.Ala1781Asp
ENST00000371385.8:c.4316C>A	ENSP00000360438.4:p.Ala1439Asp
ENST00000674738.1:c.3897C>A
ENST00000674827.1:c.3458C>A	ENSP00000502523.1:p.Ala1153Asp
ENST00000675218.1:c.4418C>A	ENSP00000501910.1:p.Ala1473Asp
ENST00000675487.1:c.*1275C>A	ENSP00000502340.1:n.*1275C>A
ENST00000675718.1:c.4611C>A
ENST00000260766.7:c.5342C>A	ENSP00000260766.3:p.Ala1781Asp
ENST00000371375.1:c.4418C>A	ENSP00000360426.1:p.Ala1473Asp
ENST00000371380.7:c.5342C>A	ENSP00000360431.2:p.Ala1781Asp
ENST00000371385.7:c.4418C>A	ENSP00000360438.3:p.Ala1473Asp
NM_001165979.2:c.4418C>A	NP_001159451.1:p.Ala1473Asp
NM_001288989.1:c.5294C>A	NP_001275918.1:p.Ala1765Asp
NM_016341.3:c.5342C>A	NP_057425.3:p.Ala1781Asp
XM_006717885.2:c.5384C>A	XP_006717948.1:p.Ala1795Asp
XM_006717886.2:c.5384C>A	XP_006717949.1:p.Ala1795Asp
XM_006717888.2:c.5381C>A	XP_006717951.1:p.Ala1794Asp
XM_006717889.2:c.5336C>A	XP_006717952.1:p.Ala1779Asp
XM_006717890.1:c.4460C>A	XP_006717953.1:p.Ala1487Asp
XM_011539849.1:c.5384C>A	XP_011538151.1:p.Ala1795Asp
XM_011539850.1:c.4229C>A	XP_011538152.1:p.Ala1410Asp
XM_006717885.4:c.5384C>A	XP_006717948.1:p.Ala1795Asp
XM_006717888.4:c.5381C>A	XP_006717951.1:p.Ala1794Asp
XM_006717889.4:c.5336C>A	XP_006717952.1:p.Ala1779Asp
XM_006717890.3:c.4460C>A	XP_006717953.1:p.Ala1487Asp
XM_011539849.3:c.5384C>A	XP_011538151.1:p.Ala1795Asp
XM_011539850.3:c.4229C>A	XP_011538152.1:p.Ala1410Asp
XM_017016310.2:c.5384C>A	XP_016871799.1:p.Ala1795Asp
XM_017016311.2:c.5384C>A	XP_016871800.1:p.Ala1795Asp
XM_017016312.2:c.4370C>A	XP_016871801.1:p.Ala1457Asp
NM_001288989.2:c.5294C>A	NP_001275918.1:p.Ala1765Asp
NM_016341.4:c.5342C>A MANE Select	NP_057425.3:p.Ala1781Asp