Canonical Allele Identifier: CA470807775

Gene: PLCE1

Linked Data

• MyVariant Identifiers: chr10:g.96053389T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94293632T>A , CM000672.2:g.94293632T>A	GRCh38
NC_000010.10:g.96053389T>A , CM000672.1:g.96053389T>A	GRCh37
NC_000010.9:g.96043379T>A	NCBI36
NG_015799.1:g.304644T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.4236T>A	ENSP00000360426.1:p.Ser1412=
ENST00000685253.1:c.*1703T>A	ENSP00000509405.1:n.*1703T>A
ENST00000685889.1:n.1895T>A
ENST00000686807.1:n.579T>A
ENST00000686954.1:c.*444T>A	ENSP00000508416.1:n.*444T>A
ENST00000688810.1:c.4188T>A	ENSP00000509140.1:p.Ser1396=
ENST00000689233.1:n.9368T>A
ENST00000690340.1:n.2833T>A
ENST00000692286.1:c.5036-4747T>A	ENSP00000509490.1:n.5036-4747T>A
ENST00000692396.1:c.5112T>A	ENSP00000508605.1:p.Ser1704=
ENST00000371380.8:c.5160T>A MANE Select	ENSP00000360431.2:p.Ser1720=
ENST00000371385.8:c.4134T>A	ENSP00000360438.4:p.Ser1378=
ENST00000674738.1:c.3715T>A
ENST00000674827.1:c.3276T>A	ENSP00000502523.1:p.Ser1092=
ENST00000675218.1:c.4236T>A	ENSP00000501910.1:p.Ser1412=
ENST00000675487.1:c.*1093T>A	ENSP00000502340.1:n.*1093T>A
ENST00000675718.1:c.4429T>A
ENST00000676102.1:c.4005T>A	ENSP00000502811.1:p.Ser1335=
ENST00000260766.7:c.5160T>A	ENSP00000260766.3:p.Ser1720=
ENST00000371375.1:c.4236T>A	ENSP00000360426.1:p.Ser1412=
ENST00000371380.7:c.5160T>A	ENSP00000360431.2:p.Ser1720=
ENST00000371385.7:c.4236T>A	ENSP00000360438.3:p.Ser1412=
NM_001165979.2:c.4236T>A	NP_001159451.1:p.Ser1412=
NM_001288989.1:c.5112T>A	NP_001275918.1:p.Ser1704=
NM_016341.3:c.5160T>A	NP_057425.3:p.Ser1720=
XM_006717885.2:c.5202T>A	XP_006717948.1:p.Ser1734=
XM_006717886.2:c.5202T>A	XP_006717949.1:p.Ser1734=
XM_006717888.2:c.5199T>A	XP_006717951.1:p.Ser1733=
XM_006717889.2:c.5154T>A	XP_006717952.1:p.Ser1718=
XM_006717890.1:c.4278T>A	XP_006717953.1:p.Ser1426=
XM_011539849.1:c.5202T>A	XP_011538151.1:p.Ser1734=
XM_011539850.1:c.4047T>A	XP_011538152.1:p.Ser1349=
XM_006717885.4:c.5202T>A	XP_006717948.1:p.Ser1734=
XM_006717888.4:c.5199T>A	XP_006717951.1:p.Ser1733=
XM_006717889.4:c.5154T>A	XP_006717952.1:p.Ser1718=
XM_006717890.3:c.4278T>A	XP_006717953.1:p.Ser1426=
XM_011539849.3:c.5202T>A	XP_011538151.1:p.Ser1734=
XM_011539850.3:c.4047T>A	XP_011538152.1:p.Ser1349=
XM_017016310.2:c.5202T>A	XP_016871799.1:p.Ser1734=
XM_017016311.2:c.5202T>A	XP_016871800.1:p.Ser1734=
XM_017016312.2:c.4188T>A	XP_016871801.1:p.Ser1396=
NM_001288989.2:c.5112T>A	NP_001275918.1:p.Ser1704=
NM_016341.4:c.5160T>A MANE Select	NP_057425.3:p.Ser1720=