Canonical Allele Identifier: CA377642123

Gene: PLCE1

Linked Data

• MyVariant Identifiers: chr10:g.96058358C>A (hg19) ; chr10:g.94298601C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298601C>A , CM000672.2:g.94298601C>A	GRCh38
NC_000010.10:g.96058358C>A , CM000672.1:g.96058358C>A	GRCh37
NC_000010.9:g.96048348C>A	NCBI36
NG_015799.1:g.309613C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000371375.2:c.4466C>A	ENSP00000360426.1:p.Ser1489Tyr
ENST00000685253.1:c.*1933C>A	ENSP00000509405.1:n.*1933C>A
ENST00000685889.1:n.2125C>A
ENST00000686807.1:n.809C>A
ENST00000686954.1:c.*674C>A	ENSP00000508416.1:n.*674C>A
ENST00000688810.1:c.4418C>A	ENSP00000509140.1:p.Ser1473Tyr
ENST00000689233.1:n.9598C>A
ENST00000690340.1:n.3063C>A
ENST00000692286.1:c.5258C>A	ENSP00000509490.1:p.Ser1753Tyr
ENST00000692396.1:c.5342C>A	ENSP00000508605.1:p.Ser1781Tyr
ENST00000371380.8:c.5390C>A MANE Select	ENSP00000360431.2:p.Ser1797Tyr
ENST00000371385.8:c.4364C>A	ENSP00000360438.4:p.Ser1455Tyr
ENST00000674738.1:c.3945C>A
ENST00000674827.1:c.3506C>A	ENSP00000502523.1:p.Ser1169Tyr
ENST00000675218.1:c.4466C>A	ENSP00000501910.1:p.Ser1489Tyr
ENST00000675487.1:c.*1323C>A	ENSP00000502340.1:n.*1323C>A
ENST00000675718.1:c.4659C>A
ENST00000260766.7:c.5390C>A	ENSP00000260766.3:p.Ser1797Tyr
ENST00000371375.1:c.4466C>A	ENSP00000360426.1:p.Ser1489Tyr
ENST00000371380.7:c.5390C>A	ENSP00000360431.2:p.Ser1797Tyr
ENST00000371385.7:c.4466C>A	ENSP00000360438.3:p.Ser1489Tyr
NM_001165979.2:c.4466C>A	NP_001159451.1:p.Ser1489Tyr
NM_001288989.1:c.5342C>A	NP_001275918.1:p.Ser1781Tyr
NM_016341.3:c.5390C>A	NP_057425.3:p.Ser1797Tyr
XM_006717885.2:c.5432C>A	XP_006717948.1:p.Ser1811Tyr
XM_006717886.2:c.5432C>A	XP_006717949.1:p.Ser1811Tyr
XM_006717888.2:c.5429C>A	XP_006717951.1:p.Ser1810Tyr
XM_006717889.2:c.5384C>A	XP_006717952.1:p.Ser1795Tyr
XM_006717890.1:c.4508C>A	XP_006717953.1:p.Ser1503Tyr
XM_011539849.1:c.5432C>A	XP_011538151.1:p.Ser1811Tyr
XM_011539850.1:c.4277C>A	XP_011538152.1:p.Ser1426Tyr
XM_006717885.4:c.5432C>A	XP_006717948.1:p.Ser1811Tyr
XM_006717888.4:c.5429C>A	XP_006717951.1:p.Ser1810Tyr
XM_006717889.4:c.5384C>A	XP_006717952.1:p.Ser1795Tyr
XM_006717890.3:c.4508C>A	XP_006717953.1:p.Ser1503Tyr
XM_011539849.3:c.5432C>A	XP_011538151.1:p.Ser1811Tyr
XM_011539850.3:c.4277C>A	XP_011538152.1:p.Ser1426Tyr
XM_017016310.2:c.5432C>A	XP_016871799.1:p.Ser1811Tyr
XM_017016311.2:c.5432C>A	XP_016871800.1:p.Ser1811Tyr
XM_017016312.2:c.4418C>A	XP_016871801.1:p.Ser1473Tyr
NM_001288989.2:c.5342C>A	NP_001275918.1:p.Ser1781Tyr
NM_016341.4:c.5390C>A MANE Select	NP_057425.3:p.Ser1797Tyr