Canonical Allele Identifier: CA377642026
Gene: PLCE1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94298555T>G , CM000672.2:g.94298555T>G GRCh38
NC_000010.10:g.96058312T>G , CM000672.1:g.96058312T>G GRCh37
NC_000010.9:g.96048302T>G NCBI36
NG_015799.1:g.309567T>G

Transcript Alleles

HGVS Amino-acid change
NM_001165979.2:c.4420T>G NP_001159451.1:p.Cys1474Gly
NM_001288989.1:c.5296T>G NP_001275918.1:p.Cys1766Gly
NM_016341.3:c.5344T>G NP_057425.3:p.Cys1782Gly
XM_006717885.2:c.5386T>G XP_006717948.1:p.Cys1796Gly
XM_006717886.2:c.5386T>G XP_006717949.1:p.Cys1796Gly
XM_006717888.2:c.5383T>G XP_006717951.1:p.Cys1795Gly
XM_006717889.2:c.5338T>G XP_006717952.1:p.Cys1780Gly
XM_006717890.1:c.4462T>G XP_006717953.1:p.Cys1488Gly
XM_011539849.1:c.5386T>G XP_011538151.1:p.Cys1796Gly
XM_011539850.1:c.4231T>G XP_011538152.1:p.Cys1411Gly
XM_006717885.4:c.5386T>G XP_006717948.1:p.Cys1796Gly
XM_006717888.4:c.5383T>G XP_006717951.1:p.Cys1795Gly
XM_006717889.4:c.5338T>G XP_006717952.1:p.Cys1780Gly
XM_006717890.3:c.4462T>G XP_006717953.1:p.Cys1488Gly
XM_011539849.3:c.5386T>G XP_011538151.1:p.Cys1796Gly
XM_011539850.3:c.4231T>G XP_011538152.1:p.Cys1411Gly
XM_017016310.2:c.5386T>G XP_016871799.1:p.Cys1796Gly
XM_017016311.2:c.5386T>G XP_016871800.1:p.Cys1796Gly
XM_017016312.2:c.4372T>G XP_016871801.1:p.Cys1458Gly
NM_001288989.2:c.5296T>G NP_001275918.1:p.Cys1766Gly
NM_016341.4:c.5344T>G MANE Select NP_057425.3:p.Cys1782Gly
ENST00000260766.7:c.5344T>G ENSP00000260766.3:p.Cys1782Gly
ENST00000371375.1:n.4420T>G ENSP00000360426.1:p.Cys1474Gly
ENST00000371380.7:c.5344T>G ENSP00000360431.2:p.Cys1782Gly
ENST00000371385.7:c.4420T>G ENSP00000360438.3:p.Cys1474Gly