Canonical Allele Identifier: CA1928998435
Gene: PLCE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94298551C= , CM000672.2:g.94298551C= GRCh38
NC_000010.10:g.96058308C= , CM000672.1:g.96058308C= GRCh37
NC_000010.9:g.96048298C= NCBI36
NG_015799.1:g.309563C=

Transcript Alleles

HGVS Amino-acid change
ENST00000371375.2:c.4416C= ENSP00000360426.1:p.Thr1472=
ENST00000685253.1:c.*1883C= ENSP00000509405.1:n.*1883C=
ENST00000685889.1:n.2075C=
ENST00000686807.1:n.759C=
ENST00000686954.1:c.*624C= ENSP00000508416.1:n.*624C=
ENST00000688810.1:c.4368C= ENSP00000509140.1:p.Thr1456=
ENST00000689233.1:n.9548C=
ENST00000690340.1:n.3013C=
ENST00000692286.1:c.5208C= ENSP00000509490.1:p.Thr1736=
ENST00000692396.1:c.5292C= ENSP00000508605.1:p.Thr1764=
ENST00000371380.8:c.5340C= MANE Select ENSP00000360431.2:p.Thr1780=
ENST00000371385.8:c.4314C= ENSP00000360438.4:p.Thr1438=
ENST00000674738.1:c.3895C=
ENST00000674827.1:c.3456C= ENSP00000502523.1:p.Thr1152=
ENST00000675218.1:c.4416C= ENSP00000501910.1:p.Thr1472=
ENST00000675487.1:c.*1273C= ENSP00000502340.1:n.*1273C=
ENST00000675718.1:c.4609C=
ENST00000260766.7:c.5340C= ENSP00000260766.3:p.Thr1780=
ENST00000371375.1:c.4416C= ENSP00000360426.1:p.Thr1472=
ENST00000371380.7:c.5340C= ENSP00000360431.2:p.Thr1780=
ENST00000371385.7:c.4416C= ENSP00000360438.3:p.Thr1472=
NM_001165979.2:c.4416C= NP_001159451.1:p.Thr1472=
NM_001288989.1:c.5292C= NP_001275918.1:p.Thr1764=
NM_016341.3:c.5340C= NP_057425.3:p.Thr1780=
XM_006717885.2:c.5382C= XP_006717948.1:p.Thr1794=
XM_006717886.2:c.5382C= XP_006717949.1:p.Thr1794=
XM_006717888.2:c.5379C= XP_006717951.1:p.Thr1793=
XM_006717889.2:c.5334C= XP_006717952.1:p.Thr1778=
XM_006717890.1:c.4458C= XP_006717953.1:p.Thr1486=
XM_011539849.1:c.5382C= XP_011538151.1:p.Thr1794=
XM_011539850.1:c.4227C= XP_011538152.1:p.Thr1409=
XM_006717885.4:c.5382C= XP_006717948.1:p.Thr1794=
XM_006717888.4:c.5379C= XP_006717951.1:p.Thr1793=
XM_006717889.4:c.5334C= XP_006717952.1:p.Thr1778=
XM_006717890.3:c.4458C= XP_006717953.1:p.Thr1486=
XM_011539849.3:c.5382C= XP_011538151.1:p.Thr1794=
XM_011539850.3:c.4227C= XP_011538152.1:p.Thr1409=
XM_017016310.2:c.5382C= XP_016871799.1:p.Thr1794=
XM_017016311.2:c.5382C= XP_016871800.1:p.Thr1794=
XM_017016312.2:c.4368C= XP_016871801.1:p.Thr1456=
NM_001288989.2:c.5292C= NP_001275918.1:p.Thr1764=
NM_016341.4:c.5340C= MANE Select NP_057425.3:p.Thr1780=