Canonical Allele Identifier: CA377641903

Gene: PLCE1

Linked Data

• MyVariant Identifiers: chr10:g.96058253A>C (hg19) ; chr10:g.94298496A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298496A>C , CM000672.2:g.94298496A>C	GRCh38
NC_000010.10:g.96058253A>C , CM000672.1:g.96058253A>C	GRCh37
NC_000010.9:g.96048243A>C	NCBI36
NG_015799.1:g.309508A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.4361A>C	ENSP00000360426.1:p.Glu1454Ala
ENST00000685253.1:c.*1828A>C	ENSP00000509405.1:n.*1828A>C
ENST00000685889.1:n.2020A>C
ENST00000686807.1:n.704A>C
ENST00000686954.1:c.*569A>C	ENSP00000508416.1:n.*569A>C
ENST00000688810.1:c.4313A>C	ENSP00000509140.1:p.Glu1438Ala
ENST00000689233.1:n.9493A>C
ENST00000690340.1:n.2958A>C
ENST00000692286.1:c.5153A>C	ENSP00000509490.1:p.Glu1718Ala
ENST00000692396.1:c.5237A>C	ENSP00000508605.1:p.Glu1746Ala
ENST00000371380.8:c.5285A>C MANE Select	ENSP00000360431.2:p.Glu1762Ala
ENST00000371385.8:c.4259A>C	ENSP00000360438.4:p.Glu1420Ala
ENST00000674738.1:c.3840A>C
ENST00000674827.1:c.3401A>C	ENSP00000502523.1:p.Glu1134Ala
ENST00000675218.1:c.4361A>C	ENSP00000501910.1:p.Glu1454Ala
ENST00000675487.1:c.*1218A>C	ENSP00000502340.1:n.*1218A>C
ENST00000675718.1:c.4554A>C
ENST00000260766.7:c.5285A>C	ENSP00000260766.3:p.Glu1762Ala
ENST00000371375.1:c.4361A>C	ENSP00000360426.1:p.Glu1454Ala
ENST00000371380.7:c.5285A>C	ENSP00000360431.2:p.Glu1762Ala
ENST00000371385.7:c.4361A>C	ENSP00000360438.3:p.Glu1454Ala
NM_001165979.2:c.4361A>C	NP_001159451.1:p.Glu1454Ala
NM_001288989.1:c.5237A>C	NP_001275918.1:p.Glu1746Ala
NM_016341.3:c.5285A>C	NP_057425.3:p.Glu1762Ala
XM_006717885.2:c.5327A>C	XP_006717948.1:p.Glu1776Ala
XM_006717886.2:c.5327A>C	XP_006717949.1:p.Glu1776Ala
XM_006717888.2:c.5324A>C	XP_006717951.1:p.Glu1775Ala
XM_006717889.2:c.5279A>C	XP_006717952.1:p.Glu1760Ala
XM_006717890.1:c.4403A>C	XP_006717953.1:p.Glu1468Ala
XM_011539849.1:c.5327A>C	XP_011538151.1:p.Glu1776Ala
XM_011539850.1:c.4172A>C	XP_011538152.1:p.Glu1391Ala
XM_006717885.4:c.5327A>C	XP_006717948.1:p.Glu1776Ala
XM_006717888.4:c.5324A>C	XP_006717951.1:p.Glu1775Ala
XM_006717889.4:c.5279A>C	XP_006717952.1:p.Glu1760Ala
XM_006717890.3:c.4403A>C	XP_006717953.1:p.Glu1468Ala
XM_011539849.3:c.5327A>C	XP_011538151.1:p.Glu1776Ala
XM_011539850.3:c.4172A>C	XP_011538152.1:p.Glu1391Ala
XM_017016310.2:c.5327A>C	XP_016871799.1:p.Glu1776Ala
XM_017016311.2:c.5327A>C	XP_016871800.1:p.Glu1776Ala
XM_017016312.2:c.4313A>C	XP_016871801.1:p.Glu1438Ala
NM_001288989.2:c.5237A>C	NP_001275918.1:p.Glu1746Ala
NM_016341.4:c.5285A>C MANE Select	NP_057425.3:p.Glu1762Ala