Canonical Allele Identifier: CA470986403

Gene: PLCE1

Linked Data

• MyVariant Identifiers: chr10:g.96058153C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298396C>A , CM000672.2:g.94298396C>A	GRCh38
NC_000010.10:g.96058153C>A , CM000672.1:g.96058153C>A	GRCh37
NC_000010.9:g.96048143C>A	NCBI36
NG_015799.1:g.309408C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000371375.2:c.4261C>A	ENSP00000360426.1:p.Arg1421=
ENST00000685253.1:c.*1728C>A	ENSP00000509405.1:n.*1728C>A
ENST00000685889.1:n.1920C>A
ENST00000686807.1:n.604C>A
ENST00000686954.1:c.*469C>A	ENSP00000508416.1:n.*469C>A
ENST00000688810.1:c.4213C>A	ENSP00000509140.1:p.Arg1405=
ENST00000689233.1:n.9393C>A
ENST00000690340.1:n.2858C>A
ENST00000692286.1:c.5053C>A	ENSP00000509490.1:p.Arg1685=
ENST00000692396.1:c.5137C>A	ENSP00000508605.1:p.Arg1713=
ENST00000371380.8:c.5185C>A MANE Select	ENSP00000360431.2:p.Arg1729=
ENST00000371385.8:c.4159C>A	ENSP00000360438.4:p.Arg1387=
ENST00000674738.1:c.3740C>A
ENST00000674827.1:c.3301C>A	ENSP00000502523.1:p.Arg1101=
ENST00000675218.1:c.4261C>A	ENSP00000501910.1:p.Arg1421=
ENST00000675487.1:c.*1118C>A	ENSP00000502340.1:n.*1118C>A
ENST00000675718.1:c.4454C>A
ENST00000676102.1:c.4030C>A	ENSP00000502811.1:p.Arg1344=
ENST00000260766.7:c.5185C>A	ENSP00000260766.3:p.Arg1729=
ENST00000371375.1:c.4261C>A	ENSP00000360426.1:p.Arg1421=
ENST00000371380.7:c.5185C>A	ENSP00000360431.2:p.Arg1729=
ENST00000371385.7:c.4261C>A	ENSP00000360438.3:p.Arg1421=
NM_001165979.2:c.4261C>A	NP_001159451.1:p.Arg1421=
NM_001288989.1:c.5137C>A	NP_001275918.1:p.Arg1713=
NM_016341.3:c.5185C>A	NP_057425.3:p.Arg1729=
XM_006717885.2:c.5227C>A	XP_006717948.1:p.Arg1743=
XM_006717886.2:c.5227C>A	XP_006717949.1:p.Arg1743=
XM_006717888.2:c.5224C>A	XP_006717951.1:p.Arg1742=
XM_006717889.2:c.5179C>A	XP_006717952.1:p.Arg1727=
XM_006717890.1:c.4303C>A	XP_006717953.1:p.Arg1435=
XM_011539849.1:c.5227C>A	XP_011538151.1:p.Arg1743=
XM_011539850.1:c.4072C>A	XP_011538152.1:p.Arg1358=
XM_006717885.4:c.5227C>A	XP_006717948.1:p.Arg1743=
XM_006717888.4:c.5224C>A	XP_006717951.1:p.Arg1742=
XM_006717889.4:c.5179C>A	XP_006717952.1:p.Arg1727=
XM_006717890.3:c.4303C>A	XP_006717953.1:p.Arg1435=
XM_011539849.3:c.5227C>A	XP_011538151.1:p.Arg1743=
XM_011539850.3:c.4072C>A	XP_011538152.1:p.Arg1358=
XM_017016310.2:c.5227C>A	XP_016871799.1:p.Arg1743=
XM_017016311.2:c.5227C>A	XP_016871800.1:p.Arg1743=
XM_017016312.2:c.4213C>A	XP_016871801.1:p.Arg1405=
NM_001288989.2:c.5137C>A	NP_001275918.1:p.Arg1713=
NM_016341.4:c.5185C>A MANE Select	NP_057425.3:p.Arg1729=