Canonical Allele Identifier: CA470986592
Gene: PLCE1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96058338T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94298581T>G , CM000672.2:g.94298581T>G GRCh38
NC_000010.10:g.96058338T>G , CM000672.1:g.96058338T>G GRCh37
NC_000010.9:g.96048328T>G NCBI36
NG_015799.1:g.309593T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371375.2:c.4446T>G ENSP00000360426.1:p.Ala1482=
ENST00000685253.1:c.*1913T>G ENSP00000509405.1:n.*1913T>G
ENST00000685889.1:n.2105T>G
ENST00000686807.1:n.789T>G
ENST00000686954.1:c.*654T>G ENSP00000508416.1:n.*654T>G
ENST00000688810.1:c.4398T>G ENSP00000509140.1:p.Ala1466=
ENST00000689233.1:n.9578T>G
ENST00000690340.1:n.3043T>G
ENST00000692286.1:c.5238T>G ENSP00000509490.1:p.Ala1746=
ENST00000692396.1:c.5322T>G ENSP00000508605.1:p.Ala1774=
ENST00000371380.8:c.5370T>G MANE Select ENSP00000360431.2:p.Ala1790=
ENST00000371385.8:c.4344T>G ENSP00000360438.4:p.Ala1448=
ENST00000674738.1:c.3925T>G
ENST00000674827.1:c.3486T>G ENSP00000502523.1:p.Ala1162=
ENST00000675218.1:c.4446T>G ENSP00000501910.1:p.Ala1482=
ENST00000675487.1:c.*1303T>G ENSP00000502340.1:n.*1303T>G
ENST00000675718.1:c.4639T>G
ENST00000260766.7:c.5370T>G ENSP00000260766.3:p.Ala1790=
ENST00000371375.1:c.4446T>G ENSP00000360426.1:p.Ala1482=
ENST00000371380.7:c.5370T>G ENSP00000360431.2:p.Ala1790=
ENST00000371385.7:c.4446T>G ENSP00000360438.3:p.Ala1482=
NM_001165979.2:c.4446T>G NP_001159451.1:p.Ala1482=
NM_001288989.1:c.5322T>G NP_001275918.1:p.Ala1774=
NM_016341.3:c.5370T>G NP_057425.3:p.Ala1790=
XM_006717885.2:c.5412T>G XP_006717948.1:p.Ala1804=
XM_006717886.2:c.5412T>G XP_006717949.1:p.Ala1804=
XM_006717888.2:c.5409T>G XP_006717951.1:p.Ala1803=
XM_006717889.2:c.5364T>G XP_006717952.1:p.Ala1788=
XM_006717890.1:c.4488T>G XP_006717953.1:p.Ala1496=
XM_011539849.1:c.5412T>G XP_011538151.1:p.Ala1804=
XM_011539850.1:c.4257T>G XP_011538152.1:p.Ala1419=
XM_006717885.4:c.5412T>G XP_006717948.1:p.Ala1804=
XM_006717888.4:c.5409T>G XP_006717951.1:p.Ala1803=
XM_006717889.4:c.5364T>G XP_006717952.1:p.Ala1788=
XM_006717890.3:c.4488T>G XP_006717953.1:p.Ala1496=
XM_011539849.3:c.5412T>G XP_011538151.1:p.Ala1804=
XM_011539850.3:c.4257T>G XP_011538152.1:p.Ala1419=
XM_017016310.2:c.5412T>G XP_016871799.1:p.Ala1804=
XM_017016311.2:c.5412T>G XP_016871800.1:p.Ala1804=
XM_017016312.2:c.4398T>G XP_016871801.1:p.Ala1466=
NM_001288989.2:c.5322T>G NP_001275918.1:p.Ala1774=
NM_016341.4:c.5370T>G MANE Select NP_057425.3:p.Ala1790=