Canonical Allele Identifier: CA211599825

Gene: PLCE1

Linked Data

• dbSNP Id: rs981294689
• gnomAD v2: 10-96058384-C-T
• gnomAD v4: 10-94298627-C-T
• MyVariant Identifiers: chr10:g.96058384C>T (hg19) ; chr10:g.94298627C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298627C>T , CM000672.2:g.94298627C>T	GRCh38
NC_000010.10:g.96058384C>T , CM000672.1:g.96058384C>T	GRCh37
NC_000010.9:g.96048374C>T	NCBI36
NG_015799.1:g.309639C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.4492C>T	ENSP00000360426.1:p.Leu1498Phe
ENST00000685253.1:c.*1959C>T	ENSP00000509405.1:n.*1959C>T
ENST00000685889.1:n.2151C>T
ENST00000686807.1:n.835C>T
ENST00000686954.1:c.*700C>T	ENSP00000508416.1:n.*700C>T
ENST00000688810.1:c.4444C>T	ENSP00000509140.1:p.Leu1482Phe
ENST00000689233.1:n.9624C>T
ENST00000690340.1:n.3089C>T
ENST00000692286.1:c.5284C>T	ENSP00000509490.1:p.Leu1762Phe
ENST00000692396.1:c.5368C>T	ENSP00000508605.1:p.Leu1790Phe
ENST00000371380.8:c.5416C>T MANE Select	ENSP00000360431.2:p.Leu1806Phe
ENST00000371385.8:c.4390C>T	ENSP00000360438.4:p.Leu1464Phe
ENST00000674738.1:c.3971C>T
ENST00000674827.1:c.3532C>T	ENSP00000502523.1:p.Leu1178Phe
ENST00000675218.1:c.4492C>T	ENSP00000501910.1:p.Leu1498Phe
ENST00000675487.1:c.*1349C>T	ENSP00000502340.1:n.*1349C>T
ENST00000675718.1:c.4685C>T
ENST00000260766.7:c.5416C>T	ENSP00000260766.3:p.Leu1806Phe
ENST00000371375.1:c.4492C>T	ENSP00000360426.1:p.Leu1498Phe
ENST00000371380.7:c.5416C>T	ENSP00000360431.2:p.Leu1806Phe
ENST00000371385.7:c.4492C>T	ENSP00000360438.3:p.Leu1498Phe
NM_001165979.2:c.4492C>T	NP_001159451.1:p.Leu1498Phe
NM_001288989.1:c.5368C>T	NP_001275918.1:p.Leu1790Phe
NM_016341.3:c.5416C>T	NP_057425.3:p.Leu1806Phe
XM_006717885.2:c.5458C>T	XP_006717948.1:p.Leu1820Phe
XM_006717886.2:c.5458C>T	XP_006717949.1:p.Leu1820Phe
XM_006717888.2:c.5455C>T	XP_006717951.1:p.Leu1819Phe
XM_006717889.2:c.5410C>T	XP_006717952.1:p.Leu1804Phe
XM_006717890.1:c.4534C>T	XP_006717953.1:p.Leu1512Phe
XM_011539849.1:c.5458C>T	XP_011538151.1:p.Leu1820Phe
XM_011539850.1:c.4303C>T	XP_011538152.1:p.Leu1435Phe
XM_006717885.4:c.5458C>T	XP_006717948.1:p.Leu1820Phe
XM_006717888.4:c.5455C>T	XP_006717951.1:p.Leu1819Phe
XM_006717889.4:c.5410C>T	XP_006717952.1:p.Leu1804Phe
XM_006717890.3:c.4534C>T	XP_006717953.1:p.Leu1512Phe
XM_011539849.3:c.5458C>T	XP_011538151.1:p.Leu1820Phe
XM_011539850.3:c.4303C>T	XP_011538152.1:p.Leu1435Phe
XM_017016310.2:c.5458C>T	XP_016871799.1:p.Leu1820Phe
XM_017016311.2:c.5458C>T	XP_016871800.1:p.Leu1820Phe
XM_017016312.2:c.4444C>T	XP_016871801.1:p.Leu1482Phe
NM_001288989.2:c.5368C>T	NP_001275918.1:p.Leu1790Phe
NM_016341.4:c.5416C>T MANE Select	NP_057425.3:p.Leu1806Phe