Canonical Allele Identifier: CA377641807
Gene: PLCE1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94298454T>C , CM000672.2:g.94298454T>C GRCh38
NC_000010.10:g.96058211T>C , CM000672.1:g.96058211T>C GRCh37
NC_000010.9:g.96048201T>C NCBI36
NG_015799.1:g.309466T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000371380.8:c.5243T>C MANE Select ENSP00000360431.2:p.Ile1748Thr
ENST00000371385.8:c.4217T>C ENSP00000360438.4:p.Ile1406Thr
ENST00000674738.1:n.3798T>C
ENST00000674827.1:n.3359T>C ENSP00000502523.1:p.Ile1120Thr
ENST00000675218.1:n.4319T>C ENSP00000501910.1:p.Ile1440Thr
ENST00000675487.1:c.*1176T>C ENSP00000502340.1:p.=
ENST00000675718.1:n.4512T>C
ENST00000676102.1:c.4088T>C ENSP00000502811.1:p.Ile1363Thr
ENST00000260766.7:c.5243T>C ENSP00000260766.3:p.Ile1748Thr
ENST00000371375.1:n.4319T>C ENSP00000360426.1:p.Ile1440Thr
ENST00000371380.7:c.5243T>C ENSP00000360431.2:p.Ile1748Thr
ENST00000371385.7:c.4319T>C ENSP00000360438.3:p.Ile1440Thr
NM_001165979.2:c.4319T>C NP_001159451.1:p.Ile1440Thr
NM_001288989.1:c.5195T>C NP_001275918.1:p.Ile1732Thr
NM_016341.3:c.5243T>C NP_057425.3:p.Ile1748Thr
XM_006717885.2:c.5285T>C XP_006717948.1:p.Ile1762Thr
XM_006717886.2:c.5285T>C XP_006717949.1:p.Ile1762Thr
XM_006717888.2:c.5282T>C XP_006717951.1:p.Ile1761Thr
XM_006717889.2:c.5237T>C XP_006717952.1:p.Ile1746Thr
XM_006717890.1:c.4361T>C XP_006717953.1:p.Ile1454Thr
XM_011539849.1:c.5285T>C XP_011538151.1:p.Ile1762Thr
XM_011539850.1:c.4130T>C XP_011538152.1:p.Ile1377Thr
XM_006717885.4:c.5285T>C XP_006717948.1:p.Ile1762Thr
XM_006717888.4:c.5282T>C XP_006717951.1:p.Ile1761Thr
XM_006717889.4:c.5237T>C XP_006717952.1:p.Ile1746Thr
XM_006717890.3:c.4361T>C XP_006717953.1:p.Ile1454Thr
XM_011539849.3:c.5285T>C XP_011538151.1:p.Ile1762Thr
XM_011539850.3:c.4130T>C XP_011538152.1:p.Ile1377Thr
XM_017016310.2:c.5285T>C XP_016871799.1:p.Ile1762Thr
XM_017016311.2:c.5285T>C XP_016871800.1:p.Ile1762Thr
XM_017016312.2:c.4271T>C XP_016871801.1:p.Ile1424Thr
NM_001288989.2:c.5195T>C NP_001275918.1:p.Ile1732Thr
NM_016341.4:c.5243T>C MANE Select NP_057425.3:p.Ile1748Thr