Canonical Allele Identifier: CA470986553
Gene: PLCE1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96058299C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94298542C>G , CM000672.2:g.94298542C>G GRCh38
NC_000010.10:g.96058299C>G , CM000672.1:g.96058299C>G GRCh37
NC_000010.9:g.96048289C>G NCBI36
NG_015799.1:g.309554C>G

Transcript Alleles

HGVS Amino-acid change
NM_001165979.2:c.4407C>G NP_001159451.1:p.Thr1469=
NM_001288989.1:c.5283C>G NP_001275918.1:p.Thr1761=
NM_016341.3:c.5331C>G NP_057425.3:p.Thr1777=
XM_006717885.2:c.5373C>G XP_006717948.1:p.Thr1791=
XM_006717886.2:c.5373C>G XP_006717949.1:p.Thr1791=
XM_006717888.2:c.5370C>G XP_006717951.1:p.Thr1790=
XM_006717889.2:c.5325C>G XP_006717952.1:p.Thr1775=
XM_006717890.1:c.4449C>G XP_006717953.1:p.Thr1483=
XM_011539849.1:c.5373C>G XP_011538151.1:p.Thr1791=
XM_011539850.1:c.4218C>G XP_011538152.1:p.Thr1406=
XM_006717885.4:c.5373C>G XP_006717948.1:p.Thr1791=
XM_006717888.4:c.5370C>G XP_006717951.1:p.Thr1790=
XM_006717889.4:c.5325C>G XP_006717952.1:p.Thr1775=
XM_006717890.3:c.4449C>G XP_006717953.1:p.Thr1483=
XM_011539849.3:c.5373C>G XP_011538151.1:p.Thr1791=
XM_011539850.3:c.4218C>G XP_011538152.1:p.Thr1406=
XM_017016310.2:c.5373C>G XP_016871799.1:p.Thr1791=
XM_017016311.2:c.5373C>G XP_016871800.1:p.Thr1791=
XM_017016312.2:c.4359C>G XP_016871801.1:p.Thr1453=
NM_001288989.2:c.5283C>G NP_001275918.1:p.Thr1761=
NM_016341.4:c.5331C>G MANE Select NP_057425.3:p.Thr1777=
ENST00000260766.7:c.5331C>G ENSP00000260766.3:p.Thr1777=
ENST00000371375.1:n.4407C>G ENSP00000360426.1:p.Thr1469=
ENST00000371380.7:c.5331C>G ENSP00000360431.2:p.Thr1777=
ENST00000371385.7:c.4407C>G ENSP00000360438.3:p.Thr1469=