Canonical Allele Identifier: CA470986447
Gene: PLCE1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96058197G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94298440G>T , CM000672.2:g.94298440G>T GRCh38
NC_000010.10:g.96058197G>T , CM000672.1:g.96058197G>T GRCh37
NC_000010.9:g.96048187G>T NCBI36
NG_015799.1:g.309452G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371375.2:c.4305G>T ENSP00000360426.1:p.Thr1435=
ENST00000685253.1:c.*1772G>T ENSP00000509405.1:n.*1772G>T
ENST00000685889.1:n.1964G>T
ENST00000686807.1:n.648G>T
ENST00000686954.1:c.*513G>T ENSP00000508416.1:n.*513G>T
ENST00000688810.1:c.4257G>T ENSP00000509140.1:p.Thr1419=
ENST00000689233.1:n.9437G>T
ENST00000690340.1:n.2902G>T
ENST00000692286.1:c.5097G>T ENSP00000509490.1:p.Thr1699=
ENST00000692396.1:c.5181G>T ENSP00000508605.1:p.Thr1727=
ENST00000371380.8:c.5229G>T MANE Select ENSP00000360431.2:p.Thr1743=
ENST00000371385.8:c.4203G>T ENSP00000360438.4:p.Thr1401=
ENST00000674738.1:c.3784G>T
ENST00000674827.1:c.3345G>T ENSP00000502523.1:p.Thr1115=
ENST00000675218.1:c.4305G>T ENSP00000501910.1:p.Thr1435=
ENST00000675487.1:c.*1162G>T ENSP00000502340.1:n.*1162G>T
ENST00000675718.1:c.4498G>T
ENST00000676102.1:c.4074G>T ENSP00000502811.1:p.Thr1358=
ENST00000260766.7:c.5229G>T ENSP00000260766.3:p.Thr1743=
ENST00000371375.1:c.4305G>T ENSP00000360426.1:p.Thr1435=
ENST00000371380.7:c.5229G>T ENSP00000360431.2:p.Thr1743=
ENST00000371385.7:c.4305G>T ENSP00000360438.3:p.Thr1435=
NM_001165979.2:c.4305G>T NP_001159451.1:p.Thr1435=
NM_001288989.1:c.5181G>T NP_001275918.1:p.Thr1727=
NM_016341.3:c.5229G>T NP_057425.3:p.Thr1743=
XM_006717885.2:c.5271G>T XP_006717948.1:p.Thr1757=
XM_006717886.2:c.5271G>T XP_006717949.1:p.Thr1757=
XM_006717888.2:c.5268G>T XP_006717951.1:p.Thr1756=
XM_006717889.2:c.5223G>T XP_006717952.1:p.Thr1741=
XM_006717890.1:c.4347G>T XP_006717953.1:p.Thr1449=
XM_011539849.1:c.5271G>T XP_011538151.1:p.Thr1757=
XM_011539850.1:c.4116G>T XP_011538152.1:p.Thr1372=
XM_006717885.4:c.5271G>T XP_006717948.1:p.Thr1757=
XM_006717888.4:c.5268G>T XP_006717951.1:p.Thr1756=
XM_006717889.4:c.5223G>T XP_006717952.1:p.Thr1741=
XM_006717890.3:c.4347G>T XP_006717953.1:p.Thr1449=
XM_011539849.3:c.5271G>T XP_011538151.1:p.Thr1757=
XM_011539850.3:c.4116G>T XP_011538152.1:p.Thr1372=
XM_017016310.2:c.5271G>T XP_016871799.1:p.Thr1757=
XM_017016311.2:c.5271G>T XP_016871800.1:p.Thr1757=
XM_017016312.2:c.4257G>T XP_016871801.1:p.Thr1419=
NM_001288989.2:c.5181G>T NP_001275918.1:p.Thr1727=
NM_016341.4:c.5229G>T MANE Select NP_057425.3:p.Thr1743=