Canonical Allele Identifier: CA377642089

Gene: PLCE1

Linked Data

• MyVariant Identifiers: chr10:g.96058342A>T (hg19) ; chr10:g.94298585A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298585A>T , CM000672.2:g.94298585A>T	GRCh38
NC_000010.10:g.96058342A>T , CM000672.1:g.96058342A>T	GRCh37
NC_000010.9:g.96048332A>T	NCBI36
NG_015799.1:g.309597A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371375.2:c.4450A>T	ENSP00000360426.1:p.Thr1484Ser
ENST00000685253.1:c.*1917A>T	ENSP00000509405.1:n.*1917A>T
ENST00000685889.1:n.2109A>T
ENST00000686807.1:n.793A>T
ENST00000686954.1:c.*658A>T	ENSP00000508416.1:n.*658A>T
ENST00000688810.1:c.4402A>T	ENSP00000509140.1:p.Thr1468Ser
ENST00000689233.1:n.9582A>T
ENST00000690340.1:n.3047A>T
ENST00000692286.1:c.5242A>T	ENSP00000509490.1:p.Thr1748Ser
ENST00000692396.1:c.5326A>T	ENSP00000508605.1:p.Thr1776Ser
ENST00000371380.8:c.5374A>T MANE Select	ENSP00000360431.2:p.Thr1792Ser
ENST00000371385.8:c.4348A>T	ENSP00000360438.4:p.Thr1450Ser
ENST00000674738.1:c.3929A>T
ENST00000674827.1:c.3490A>T	ENSP00000502523.1:p.Thr1164Ser
ENST00000675218.1:c.4450A>T	ENSP00000501910.1:p.Thr1484Ser
ENST00000675487.1:c.*1307A>T	ENSP00000502340.1:n.*1307A>T
ENST00000675718.1:c.4643A>T
ENST00000260766.7:c.5374A>T	ENSP00000260766.3:p.Thr1792Ser
ENST00000371375.1:c.4450A>T	ENSP00000360426.1:p.Thr1484Ser
ENST00000371380.7:c.5374A>T	ENSP00000360431.2:p.Thr1792Ser
ENST00000371385.7:c.4450A>T	ENSP00000360438.3:p.Thr1484Ser
NM_001165979.2:c.4450A>T	NP_001159451.1:p.Thr1484Ser
NM_001288989.1:c.5326A>T	NP_001275918.1:p.Thr1776Ser
NM_016341.3:c.5374A>T	NP_057425.3:p.Thr1792Ser
XM_006717885.2:c.5416A>T	XP_006717948.1:p.Thr1806Ser
XM_006717886.2:c.5416A>T	XP_006717949.1:p.Thr1806Ser
XM_006717888.2:c.5413A>T	XP_006717951.1:p.Thr1805Ser
XM_006717889.2:c.5368A>T	XP_006717952.1:p.Thr1790Ser
XM_006717890.1:c.4492A>T	XP_006717953.1:p.Thr1498Ser
XM_011539849.1:c.5416A>T	XP_011538151.1:p.Thr1806Ser
XM_011539850.1:c.4261A>T	XP_011538152.1:p.Thr1421Ser
XM_006717885.4:c.5416A>T	XP_006717948.1:p.Thr1806Ser
XM_006717888.4:c.5413A>T	XP_006717951.1:p.Thr1805Ser
XM_006717889.4:c.5368A>T	XP_006717952.1:p.Thr1790Ser
XM_006717890.3:c.4492A>T	XP_006717953.1:p.Thr1498Ser
XM_011539849.3:c.5416A>T	XP_011538151.1:p.Thr1806Ser
XM_011539850.3:c.4261A>T	XP_011538152.1:p.Thr1421Ser
XM_017016310.2:c.5416A>T	XP_016871799.1:p.Thr1806Ser
XM_017016311.2:c.5416A>T	XP_016871800.1:p.Thr1806Ser
XM_017016312.2:c.4402A>T	XP_016871801.1:p.Thr1468Ser
NM_001288989.2:c.5326A>T	NP_001275918.1:p.Thr1776Ser
NM_016341.4:c.5374A>T MANE Select	NP_057425.3:p.Thr1792Ser