Canonical Allele Identifier: CA377642058
Gene: PLCE1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94298570A>G , CM000672.2:g.94298570A>G GRCh38
NC_000010.10:g.96058327A>G , CM000672.1:g.96058327A>G GRCh37
NC_000010.9:g.96048317A>G NCBI36
NG_015799.1:g.309582A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371380.8:c.5359A>G MANE Select ENSP00000360431.2:p.Thr1787Ala
ENST00000371385.8:c.4333A>G ENSP00000360438.4:p.Thr1445Ala
ENST00000674738.1:n.3914A>G
ENST00000674827.1:n.3475A>G ENSP00000502523.1:p.Thr1159Ala
ENST00000675218.1:n.4435A>G ENSP00000501910.1:p.Thr1479Ala
ENST00000675487.1:c.*1292A>G ENSP00000502340.1:p.=
ENST00000675718.1:n.4628A>G
ENST00000260766.7:c.5359A>G ENSP00000260766.3:p.Thr1787Ala
ENST00000371375.1:n.4435A>G ENSP00000360426.1:p.Thr1479Ala
ENST00000371380.7:c.5359A>G ENSP00000360431.2:p.Thr1787Ala
ENST00000371385.7:c.4435A>G ENSP00000360438.3:p.Thr1479Ala
NM_001165979.2:c.4435A>G NP_001159451.1:p.Thr1479Ala
NM_001288989.1:c.5311A>G NP_001275918.1:p.Thr1771Ala
NM_016341.3:c.5359A>G NP_057425.3:p.Thr1787Ala
XM_006717885.2:c.5401A>G XP_006717948.1:p.Thr1801Ala
XM_006717886.2:c.5401A>G XP_006717949.1:p.Thr1801Ala
XM_006717888.2:c.5398A>G XP_006717951.1:p.Thr1800Ala
XM_006717889.2:c.5353A>G XP_006717952.1:p.Thr1785Ala
XM_006717890.1:c.4477A>G XP_006717953.1:p.Thr1493Ala
XM_011539849.1:c.5401A>G XP_011538151.1:p.Thr1801Ala
XM_011539850.1:c.4246A>G XP_011538152.1:p.Thr1416Ala
XM_006717885.4:c.5401A>G XP_006717948.1:p.Thr1801Ala
XM_006717888.4:c.5398A>G XP_006717951.1:p.Thr1800Ala
XM_006717889.4:c.5353A>G XP_006717952.1:p.Thr1785Ala
XM_006717890.3:c.4477A>G XP_006717953.1:p.Thr1493Ala
XM_011539849.3:c.5401A>G XP_011538151.1:p.Thr1801Ala
XM_011539850.3:c.4246A>G XP_011538152.1:p.Thr1416Ala
XM_017016310.2:c.5401A>G XP_016871799.1:p.Thr1801Ala
XM_017016311.2:c.5401A>G XP_016871800.1:p.Thr1801Ala
XM_017016312.2:c.4387A>G XP_016871801.1:p.Thr1463Ala
NM_001288989.2:c.5311A>G NP_001275918.1:p.Thr1771Ala
NM_016341.4:c.5359A>G MANE Select NP_057425.3:p.Thr1787Ala