Canonical Allele Identifier: CA377641899

Gene: PLCE1

Linked Data

• MyVariant Identifiers: chr10:g.96058252G>C (hg19) ; chr10:g.94298495G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298495G>C , CM000672.2:g.94298495G>C	GRCh38
NC_000010.10:g.96058252G>C , CM000672.1:g.96058252G>C	GRCh37
NC_000010.9:g.96048242G>C	NCBI36
NG_015799.1:g.309507G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000371375.2:c.4360G>C	ENSP00000360426.1:p.Glu1454Gln
ENST00000685253.1:c.*1827G>C	ENSP00000509405.1:n.*1827G>C
ENST00000685889.1:n.2019G>C
ENST00000686807.1:n.703G>C
ENST00000686954.1:c.*568G>C	ENSP00000508416.1:n.*568G>C
ENST00000688810.1:c.4312G>C	ENSP00000509140.1:p.Glu1438Gln
ENST00000689233.1:n.9492G>C
ENST00000690340.1:n.2957G>C
ENST00000692286.1:c.5152G>C	ENSP00000509490.1:p.Glu1718Gln
ENST00000692396.1:c.5236G>C	ENSP00000508605.1:p.Glu1746Gln
ENST00000371380.8:c.5284G>C MANE Select	ENSP00000360431.2:p.Glu1762Gln
ENST00000371385.8:c.4258G>C	ENSP00000360438.4:p.Glu1420Gln
ENST00000674738.1:c.3839G>C
ENST00000674827.1:c.3400G>C	ENSP00000502523.1:p.Glu1134Gln
ENST00000675218.1:c.4360G>C	ENSP00000501910.1:p.Glu1454Gln
ENST00000675487.1:c.*1217G>C	ENSP00000502340.1:n.*1217G>C
ENST00000675718.1:c.4553G>C
ENST00000260766.7:c.5284G>C	ENSP00000260766.3:p.Glu1762Gln
ENST00000371375.1:c.4360G>C	ENSP00000360426.1:p.Glu1454Gln
ENST00000371380.7:c.5284G>C	ENSP00000360431.2:p.Glu1762Gln
ENST00000371385.7:c.4360G>C	ENSP00000360438.3:p.Glu1454Gln
NM_001165979.2:c.4360G>C	NP_001159451.1:p.Glu1454Gln
NM_001288989.1:c.5236G>C	NP_001275918.1:p.Glu1746Gln
NM_016341.3:c.5284G>C	NP_057425.3:p.Glu1762Gln
XM_006717885.2:c.5326G>C	XP_006717948.1:p.Glu1776Gln
XM_006717886.2:c.5326G>C	XP_006717949.1:p.Glu1776Gln
XM_006717888.2:c.5323G>C	XP_006717951.1:p.Glu1775Gln
XM_006717889.2:c.5278G>C	XP_006717952.1:p.Glu1760Gln
XM_006717890.1:c.4402G>C	XP_006717953.1:p.Glu1468Gln
XM_011539849.1:c.5326G>C	XP_011538151.1:p.Glu1776Gln
XM_011539850.1:c.4171G>C	XP_011538152.1:p.Glu1391Gln
XM_006717885.4:c.5326G>C	XP_006717948.1:p.Glu1776Gln
XM_006717888.4:c.5323G>C	XP_006717951.1:p.Glu1775Gln
XM_006717889.4:c.5278G>C	XP_006717952.1:p.Glu1760Gln
XM_006717890.3:c.4402G>C	XP_006717953.1:p.Glu1468Gln
XM_011539849.3:c.5326G>C	XP_011538151.1:p.Glu1776Gln
XM_011539850.3:c.4171G>C	XP_011538152.1:p.Glu1391Gln
XM_017016310.2:c.5326G>C	XP_016871799.1:p.Glu1776Gln
XM_017016311.2:c.5326G>C	XP_016871800.1:p.Glu1776Gln
XM_017016312.2:c.4312G>C	XP_016871801.1:p.Glu1438Gln
NM_001288989.2:c.5236G>C	NP_001275918.1:p.Glu1746Gln
NM_016341.4:c.5284G>C MANE Select	NP_057425.3:p.Glu1762Gln