Canonical Allele Identifier: CA377641947

Gene: PLCE1

Linked Data

• MyVariant Identifiers: chr10:g.96058274G>T (hg19) ; chr10:g.94298517G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298517G>T , CM000672.2:g.94298517G>T	GRCh38
NC_000010.10:g.96058274G>T , CM000672.1:g.96058274G>T	GRCh37
NC_000010.9:g.96048264G>T	NCBI36
NG_015799.1:g.309529G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.4382G>T	ENSP00000360426.1:p.Cys1461Phe
ENST00000685253.1:c.*1849G>T	ENSP00000509405.1:n.*1849G>T
ENST00000685889.1:n.2041G>T
ENST00000686807.1:n.725G>T
ENST00000686954.1:c.*590G>T	ENSP00000508416.1:n.*590G>T
ENST00000688810.1:c.4334G>T	ENSP00000509140.1:p.Cys1445Phe
ENST00000689233.1:n.9514G>T
ENST00000690340.1:n.2979G>T
ENST00000692286.1:c.5174G>T	ENSP00000509490.1:p.Cys1725Phe
ENST00000692396.1:c.5258G>T	ENSP00000508605.1:p.Cys1753Phe
ENST00000371380.8:c.5306G>T MANE Select	ENSP00000360431.2:p.Cys1769Phe
ENST00000371385.8:c.4280G>T	ENSP00000360438.4:p.Cys1427Phe
ENST00000674738.1:c.3861G>T
ENST00000674827.1:c.3422G>T	ENSP00000502523.1:p.Cys1141Phe
ENST00000675218.1:c.4382G>T	ENSP00000501910.1:p.Cys1461Phe
ENST00000675487.1:c.*1239G>T	ENSP00000502340.1:n.*1239G>T
ENST00000675718.1:c.4575G>T
ENST00000260766.7:c.5306G>T	ENSP00000260766.3:p.Cys1769Phe
ENST00000371375.1:c.4382G>T	ENSP00000360426.1:p.Cys1461Phe
ENST00000371380.7:c.5306G>T	ENSP00000360431.2:p.Cys1769Phe
ENST00000371385.7:c.4382G>T	ENSP00000360438.3:p.Cys1461Phe
NM_001165979.2:c.4382G>T	NP_001159451.1:p.Cys1461Phe
NM_001288989.1:c.5258G>T	NP_001275918.1:p.Cys1753Phe
NM_016341.3:c.5306G>T	NP_057425.3:p.Cys1769Phe
XM_006717885.2:c.5348G>T	XP_006717948.1:p.Cys1783Phe
XM_006717886.2:c.5348G>T	XP_006717949.1:p.Cys1783Phe
XM_006717888.2:c.5345G>T	XP_006717951.1:p.Cys1782Phe
XM_006717889.2:c.5300G>T	XP_006717952.1:p.Cys1767Phe
XM_006717890.1:c.4424G>T	XP_006717953.1:p.Cys1475Phe
XM_011539849.1:c.5348G>T	XP_011538151.1:p.Cys1783Phe
XM_011539850.1:c.4193G>T	XP_011538152.1:p.Cys1398Phe
XM_006717885.4:c.5348G>T	XP_006717948.1:p.Cys1783Phe
XM_006717888.4:c.5345G>T	XP_006717951.1:p.Cys1782Phe
XM_006717889.4:c.5300G>T	XP_006717952.1:p.Cys1767Phe
XM_006717890.3:c.4424G>T	XP_006717953.1:p.Cys1475Phe
XM_011539849.3:c.5348G>T	XP_011538151.1:p.Cys1783Phe
XM_011539850.3:c.4193G>T	XP_011538152.1:p.Cys1398Phe
XM_017016310.2:c.5348G>T	XP_016871799.1:p.Cys1783Phe
XM_017016311.2:c.5348G>T	XP_016871800.1:p.Cys1783Phe
XM_017016312.2:c.4334G>T	XP_016871801.1:p.Cys1445Phe
NM_001288989.2:c.5258G>T	NP_001275918.1:p.Cys1753Phe
NM_016341.4:c.5306G>T MANE Select	NP_057425.3:p.Cys1769Phe