Canonical Allele Identifier: CA1928998382

Gene: PLCE1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298417T= , CM000672.2:g.94298417T=	GRCh38
NC_000010.10:g.96058174T= , CM000672.1:g.96058174T=	GRCh37
NC_000010.9:g.96048164T=	NCBI36
NG_015799.1:g.309429T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.4282T=	ENSP00000360426.1:p.Ser1428=
ENST00000685253.1:c.*1749T=	ENSP00000509405.1:n.*1749T=
ENST00000685889.1:n.1941T=
ENST00000686807.1:n.625T=
ENST00000686954.1:c.*490T=	ENSP00000508416.1:n.*490T=
ENST00000688810.1:c.4234T=	ENSP00000509140.1:p.Ser1412=
ENST00000689233.1:n.9414T=
ENST00000690340.1:n.2879T=
ENST00000692286.1:c.5074T=	ENSP00000509490.1:p.Ser1692=
ENST00000692396.1:c.5158T=	ENSP00000508605.1:p.Ser1720=
ENST00000371380.8:c.5206T= MANE Select	ENSP00000360431.2:p.Ser1736=
ENST00000371385.8:c.4180T=	ENSP00000360438.4:p.Ser1394=
ENST00000674738.1:c.3761T=
ENST00000674827.1:c.3322T=	ENSP00000502523.1:p.Ser1108=
ENST00000675218.1:c.4282T=	ENSP00000501910.1:p.Ser1428=
ENST00000675487.1:c.*1139T=	ENSP00000502340.1:n.*1139T=
ENST00000675718.1:c.4475T=
ENST00000676102.1:c.4051T=	ENSP00000502811.1:p.Ser1351=
ENST00000260766.7:c.5206T=	ENSP00000260766.3:p.Ser1736=
ENST00000371375.1:c.4282T=	ENSP00000360426.1:p.Ser1428=
ENST00000371380.7:c.5206T=	ENSP00000360431.2:p.Ser1736=
ENST00000371385.7:c.4282T=	ENSP00000360438.3:p.Ser1428=
NM_001165979.2:c.4282T=	NP_001159451.1:p.Ser1428=
NM_001288989.1:c.5158T=	NP_001275918.1:p.Ser1720=
NM_016341.3:c.5206T=	NP_057425.3:p.Ser1736=
XM_006717885.2:c.5248T=	XP_006717948.1:p.Ser1750=
XM_006717886.2:c.5248T=	XP_006717949.1:p.Ser1750=
XM_006717888.2:c.5245T=	XP_006717951.1:p.Ser1749=
XM_006717889.2:c.5200T=	XP_006717952.1:p.Ser1734=
XM_006717890.1:c.4324T=	XP_006717953.1:p.Ser1442=
XM_011539849.1:c.5248T=	XP_011538151.1:p.Ser1750=
XM_011539850.1:c.4093T=	XP_011538152.1:p.Ser1365=
XM_006717885.4:c.5248T=	XP_006717948.1:p.Ser1750=
XM_006717888.4:c.5245T=	XP_006717951.1:p.Ser1749=
XM_006717889.4:c.5200T=	XP_006717952.1:p.Ser1734=
XM_006717890.3:c.4324T=	XP_006717953.1:p.Ser1442=
XM_011539849.3:c.5248T=	XP_011538151.1:p.Ser1750=
XM_011539850.3:c.4093T=	XP_011538152.1:p.Ser1365=
XM_017016310.2:c.5248T=	XP_016871799.1:p.Ser1750=
XM_017016311.2:c.5248T=	XP_016871800.1:p.Ser1750=
XM_017016312.2:c.4234T=	XP_016871801.1:p.Ser1412=
NM_001288989.2:c.5158T=	NP_001275918.1:p.Ser1720=
NM_016341.4:c.5206T= MANE Select	NP_057425.3:p.Ser1736=