Canonical Allele Identifier: CA377642306

Gene: PLCE1

Linked Data

• MyVariant Identifiers: chr10:g.96058406C>T (hg19) ; chr10:g.94298649C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298649C>T , CM000672.2:g.94298649C>T	GRCh38
NC_000010.10:g.96058406C>T , CM000672.1:g.96058406C>T	GRCh37
NC_000010.9:g.96048396C>T	NCBI36
NG_015799.1:g.309661C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.4514C>T	ENSP00000360426.1:p.Ala1505Val
ENST00000685253.1:c.*1981C>T	ENSP00000509405.1:n.*1981C>T
ENST00000685889.1:n.2173C>T
ENST00000686807.1:n.857C>T
ENST00000686954.1:c.*722C>T	ENSP00000508416.1:n.*722C>T
ENST00000688810.1:c.4466C>T	ENSP00000509140.1:p.Ala1489Val
ENST00000689233.1:n.9646C>T
ENST00000690340.1:n.3111C>T
ENST00000692286.1:c.5306C>T	ENSP00000509490.1:p.Ala1769Val
ENST00000692396.1:c.5390C>T	ENSP00000508605.1:p.Ala1797Val
ENST00000371380.8:c.5438C>T MANE Select	ENSP00000360431.2:p.Ala1813Val
ENST00000371385.8:c.4412C>T	ENSP00000360438.4:p.Ala1471Val
ENST00000674738.1:c.3993C>T
ENST00000674827.1:c.3554C>T	ENSP00000502523.1:p.Ala1185Val
ENST00000675218.1:c.4514C>T	ENSP00000501910.1:p.Ala1505Val
ENST00000675487.1:c.*1371C>T	ENSP00000502340.1:n.*1371C>T
ENST00000675718.1:c.4707C>T
ENST00000260766.7:c.5438C>T	ENSP00000260766.3:p.Ala1813Val
ENST00000371375.1:c.4514C>T	ENSP00000360426.1:p.Ala1505Val
ENST00000371380.7:c.5438C>T	ENSP00000360431.2:p.Ala1813Val
ENST00000371385.7:c.4514C>T	ENSP00000360438.3:p.Ala1505Val
NM_001165979.2:c.4514C>T	NP_001159451.1:p.Ala1505Val
NM_001288989.1:c.5390C>T	NP_001275918.1:p.Ala1797Val
NM_016341.3:c.5438C>T	NP_057425.3:p.Ala1813Val
XM_006717885.2:c.5480C>T	XP_006717948.1:p.Ala1827Val
XM_006717886.2:c.5480C>T	XP_006717949.1:p.Ala1827Val
XM_006717888.2:c.5477C>T	XP_006717951.1:p.Ala1826Val
XM_006717889.2:c.5432C>T	XP_006717952.1:p.Ala1811Val
XM_006717890.1:c.4556C>T	XP_006717953.1:p.Ala1519Val
XM_011539849.1:c.5480C>T	XP_011538151.1:p.Ala1827Val
XM_011539850.1:c.4325C>T	XP_011538152.1:p.Ala1442Val
XM_006717885.4:c.5480C>T	XP_006717948.1:p.Ala1827Val
XM_006717888.4:c.5477C>T	XP_006717951.1:p.Ala1826Val
XM_006717889.4:c.5432C>T	XP_006717952.1:p.Ala1811Val
XM_006717890.3:c.4556C>T	XP_006717953.1:p.Ala1519Val
XM_011539849.3:c.5480C>T	XP_011538151.1:p.Ala1827Val
XM_011539850.3:c.4325C>T	XP_011538152.1:p.Ala1442Val
XM_017016310.2:c.5480C>T	XP_016871799.1:p.Ala1827Val
XM_017016311.2:c.5480C>T	XP_016871800.1:p.Ala1827Val
XM_017016312.2:c.4466C>T	XP_016871801.1:p.Ala1489Val
NM_001288989.2:c.5390C>T	NP_001275918.1:p.Ala1797Val
NM_016341.4:c.5438C>T MANE Select	NP_057425.3:p.Ala1813Val