Canonical Allele Identifier: CA470986466
Gene: PLCE1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96058215T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94298458T>C , CM000672.2:g.94298458T>C GRCh38
NC_000010.10:g.96058215T>C , CM000672.1:g.96058215T>C GRCh37
NC_000010.9:g.96048205T>C NCBI36
NG_015799.1:g.309470T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000371380.8:c.5247T>C MANE Select ENSP00000360431.2:p.Ile1749=
ENST00000371385.8:c.4221T>C ENSP00000360438.4:p.Ile1407=
ENST00000674738.1:n.3802T>C
ENST00000674827.1:n.3363T>C ENSP00000502523.1:p.Ile1121=
ENST00000675218.1:n.4323T>C ENSP00000501910.1:p.Ile1441=
ENST00000675487.1:c.*1180T>C ENSP00000502340.1:p.=
ENST00000675718.1:n.4516T>C
ENST00000676102.1:c.4092T>C ENSP00000502811.1:p.Ile1364=
ENST00000260766.7:c.5247T>C ENSP00000260766.3:p.Ile1749=
ENST00000371375.1:n.4323T>C ENSP00000360426.1:p.Ile1441=
ENST00000371380.7:c.5247T>C ENSP00000360431.2:p.Ile1749=
ENST00000371385.7:c.4323T>C ENSP00000360438.3:p.Ile1441=
NM_001165979.2:c.4323T>C NP_001159451.1:p.Ile1441=
NM_001288989.1:c.5199T>C NP_001275918.1:p.Ile1733=
NM_016341.3:c.5247T>C NP_057425.3:p.Ile1749=
XM_006717885.2:c.5289T>C XP_006717948.1:p.Ile1763=
XM_006717886.2:c.5289T>C XP_006717949.1:p.Ile1763=
XM_006717888.2:c.5286T>C XP_006717951.1:p.Ile1762=
XM_006717889.2:c.5241T>C XP_006717952.1:p.Ile1747=
XM_006717890.1:c.4365T>C XP_006717953.1:p.Ile1455=
XM_011539849.1:c.5289T>C XP_011538151.1:p.Ile1763=
XM_011539850.1:c.4134T>C XP_011538152.1:p.Ile1378=
XM_006717885.4:c.5289T>C XP_006717948.1:p.Ile1763=
XM_006717888.4:c.5286T>C XP_006717951.1:p.Ile1762=
XM_006717889.4:c.5241T>C XP_006717952.1:p.Ile1747=
XM_006717890.3:c.4365T>C XP_006717953.1:p.Ile1455=
XM_011539849.3:c.5289T>C XP_011538151.1:p.Ile1763=
XM_011539850.3:c.4134T>C XP_011538152.1:p.Ile1378=
XM_017016310.2:c.5289T>C XP_016871799.1:p.Ile1763=
XM_017016311.2:c.5289T>C XP_016871800.1:p.Ile1763=
XM_017016312.2:c.4275T>C XP_016871801.1:p.Ile1425=
NM_001288989.2:c.5199T>C NP_001275918.1:p.Ile1733=
NM_016341.4:c.5247T>C MANE Select NP_057425.3:p.Ile1749=