Canonical Allele Identifier: CA470986480
Gene: PLCE1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96058230T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94298473T>C , CM000672.2:g.94298473T>C GRCh38
NC_000010.10:g.96058230T>C , CM000672.1:g.96058230T>C GRCh37
NC_000010.9:g.96048220T>C NCBI36
NG_015799.1:g.309485T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000371375.2:n.4338T>C ENSP00000360426.1:p.Cys1446=
ENST00000685253.1:c.*1805T>C ENSP00000509405.1:n.*1805T>C
ENST00000685889.1:n.1997T>C
ENST00000686807.1:n.681T>C
ENST00000686954.1:c.*546T>C ENSP00000508416.1:n.*546T>C
ENST00000688810.1:n.4290T>C ENSP00000509140.1:p.Cys1430=
ENST00000689233.1:n.9470T>C
ENST00000690340.1:n.2935T>C
ENST00000692286.1:c.5130T>C ENSP00000509490.1:p.Cys1710=
ENST00000692396.1:c.5214T>C ENSP00000508605.1:p.Cys1738=
ENST00000371380.8:c.5262T>C MANE Select ENSP00000360431.2:p.Cys1754=
ENST00000371385.8:c.4236T>C ENSP00000360438.4:p.Cys1412=
ENST00000674738.1:n.3817T>C
ENST00000674827.1:n.3378T>C ENSP00000502523.1:p.Cys1126=
ENST00000675218.1:n.4338T>C ENSP00000501910.1:p.Cys1446=
ENST00000675487.1:c.*1195T>C ENSP00000502340.1:n.*1195T>C
ENST00000675718.1:n.4531T>C
ENST00000676102.1:c.4107T>C ENSP00000502811.1:p.Cys1369=
ENST00000260766.7:c.5262T>C ENSP00000260766.3:p.Cys1754=
ENST00000371375.1:n.4338T>C ENSP00000360426.1:p.Cys1446=
ENST00000371380.7:c.5262T>C ENSP00000360431.2:p.Cys1754=
ENST00000371385.7:c.4338T>C ENSP00000360438.3:p.Cys1446=
NM_001165979.2:c.4338T>C NP_001159451.1:p.Cys1446=
NM_001288989.1:c.5214T>C NP_001275918.1:p.Cys1738=
NM_016341.3:c.5262T>C NP_057425.3:p.Cys1754=
XM_006717885.2:c.5304T>C XP_006717948.1:p.Cys1768=
XM_006717886.2:c.5304T>C XP_006717949.1:p.Cys1768=
XM_006717888.2:c.5301T>C XP_006717951.1:p.Cys1767=
XM_006717889.2:c.5256T>C XP_006717952.1:p.Cys1752=
XM_006717890.1:c.4380T>C XP_006717953.1:p.Cys1460=
XM_011539849.1:c.5304T>C XP_011538151.1:p.Cys1768=
XM_011539850.1:c.4149T>C XP_011538152.1:p.Cys1383=
XM_006717885.4:c.5304T>C XP_006717948.1:p.Cys1768=
XM_006717888.4:c.5301T>C XP_006717951.1:p.Cys1767=
XM_006717889.4:c.5256T>C XP_006717952.1:p.Cys1752=
XM_006717890.3:c.4380T>C XP_006717953.1:p.Cys1460=
XM_011539849.3:c.5304T>C XP_011538151.1:p.Cys1768=
XM_011539850.3:c.4149T>C XP_011538152.1:p.Cys1383=
XM_017016310.2:c.5304T>C XP_016871799.1:p.Cys1768=
XM_017016311.2:c.5304T>C XP_016871800.1:p.Cys1768=
XM_017016312.2:c.4290T>C XP_016871801.1:p.Cys1430=
NM_001288989.2:c.5214T>C NP_001275918.1:p.Cys1738=
NM_016341.4:c.5262T>C MANE Select NP_057425.3:p.Cys1754=