Canonical Allele Identifier: CA377641905

Gene: PLCE1

Linked Data

• MyVariant Identifiers: chr10:g.96058254A>T (hg19) ; chr10:g.94298497A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298497A>T , CM000672.2:g.94298497A>T	GRCh38
NC_000010.10:g.96058254A>T , CM000672.1:g.96058254A>T	GRCh37
NC_000010.9:g.96048244A>T	NCBI36
NG_015799.1:g.309509A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371375.2:c.4362A>T	ENSP00000360426.1:p.Glu1454Asp
ENST00000685253.1:c.*1829A>T	ENSP00000509405.1:n.*1829A>T
ENST00000685889.1:n.2021A>T
ENST00000686807.1:n.705A>T
ENST00000686954.1:c.*570A>T	ENSP00000508416.1:n.*570A>T
ENST00000688810.1:c.4314A>T	ENSP00000509140.1:p.Glu1438Asp
ENST00000689233.1:n.9494A>T
ENST00000690340.1:n.2959A>T
ENST00000692286.1:c.5154A>T	ENSP00000509490.1:p.Glu1718Asp
ENST00000692396.1:c.5238A>T	ENSP00000508605.1:p.Glu1746Asp
ENST00000371380.8:c.5286A>T MANE Select	ENSP00000360431.2:p.Glu1762Asp
ENST00000371385.8:c.4260A>T	ENSP00000360438.4:p.Glu1420Asp
ENST00000674738.1:c.3841A>T
ENST00000674827.1:c.3402A>T	ENSP00000502523.1:p.Glu1134Asp
ENST00000675218.1:c.4362A>T	ENSP00000501910.1:p.Glu1454Asp
ENST00000675487.1:c.*1219A>T	ENSP00000502340.1:n.*1219A>T
ENST00000675718.1:c.4555A>T
ENST00000260766.7:c.5286A>T	ENSP00000260766.3:p.Glu1762Asp
ENST00000371375.1:c.4362A>T	ENSP00000360426.1:p.Glu1454Asp
ENST00000371380.7:c.5286A>T	ENSP00000360431.2:p.Glu1762Asp
ENST00000371385.7:c.4362A>T	ENSP00000360438.3:p.Glu1454Asp
NM_001165979.2:c.4362A>T	NP_001159451.1:p.Glu1454Asp
NM_001288989.1:c.5238A>T	NP_001275918.1:p.Glu1746Asp
NM_016341.3:c.5286A>T	NP_057425.3:p.Glu1762Asp
XM_006717885.2:c.5328A>T	XP_006717948.1:p.Glu1776Asp
XM_006717886.2:c.5328A>T	XP_006717949.1:p.Glu1776Asp
XM_006717888.2:c.5325A>T	XP_006717951.1:p.Glu1775Asp
XM_006717889.2:c.5280A>T	XP_006717952.1:p.Glu1760Asp
XM_006717890.1:c.4404A>T	XP_006717953.1:p.Glu1468Asp
XM_011539849.1:c.5328A>T	XP_011538151.1:p.Glu1776Asp
XM_011539850.1:c.4173A>T	XP_011538152.1:p.Glu1391Asp
XM_006717885.4:c.5328A>T	XP_006717948.1:p.Glu1776Asp
XM_006717888.4:c.5325A>T	XP_006717951.1:p.Glu1775Asp
XM_006717889.4:c.5280A>T	XP_006717952.1:p.Glu1760Asp
XM_006717890.3:c.4404A>T	XP_006717953.1:p.Glu1468Asp
XM_011539849.3:c.5328A>T	XP_011538151.1:p.Glu1776Asp
XM_011539850.3:c.4173A>T	XP_011538152.1:p.Glu1391Asp
XM_017016310.2:c.5328A>T	XP_016871799.1:p.Glu1776Asp
XM_017016311.2:c.5328A>T	XP_016871800.1:p.Glu1776Asp
XM_017016312.2:c.4314A>T	XP_016871801.1:p.Glu1438Asp
NM_001288989.2:c.5238A>T	NP_001275918.1:p.Glu1746Asp
NM_016341.4:c.5286A>T MANE Select	NP_057425.3:p.Glu1762Asp