Canonical Allele Identifier: CA377641789
Gene: PLCE1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94298447A>C , CM000672.2:g.94298447A>C GRCh38
NC_000010.10:g.96058204A>C , CM000672.1:g.96058204A>C GRCh37
NC_000010.9:g.96048194A>C NCBI36
NG_015799.1:g.309459A>C

Transcript Alleles

HGVS Amino-acid change
NM_001165979.2:c.4312A>C NP_001159451.1:p.Ser1438Arg
NM_001288989.1:c.5188A>C NP_001275918.1:p.Ser1730Arg
NM_016341.3:c.5236A>C NP_057425.3:p.Ser1746Arg
XM_006717885.2:c.5278A>C XP_006717948.1:p.Ser1760Arg
XM_006717886.2:c.5278A>C XP_006717949.1:p.Ser1760Arg
XM_006717888.2:c.5275A>C XP_006717951.1:p.Ser1759Arg
XM_006717889.2:c.5230A>C XP_006717952.1:p.Ser1744Arg
XM_006717890.1:c.4354A>C XP_006717953.1:p.Ser1452Arg
XM_011539849.1:c.5278A>C XP_011538151.1:p.Ser1760Arg
XM_011539850.1:c.4123A>C XP_011538152.1:p.Ser1375Arg
XM_006717885.4:c.5278A>C XP_006717948.1:p.Ser1760Arg
XM_006717888.4:c.5275A>C XP_006717951.1:p.Ser1759Arg
XM_006717889.4:c.5230A>C XP_006717952.1:p.Ser1744Arg
XM_006717890.3:c.4354A>C XP_006717953.1:p.Ser1452Arg
XM_011539849.3:c.5278A>C XP_011538151.1:p.Ser1760Arg
XM_011539850.3:c.4123A>C XP_011538152.1:p.Ser1375Arg
XM_017016310.2:c.5278A>C XP_016871799.1:p.Ser1760Arg
XM_017016311.2:c.5278A>C XP_016871800.1:p.Ser1760Arg
XM_017016312.2:c.4264A>C XP_016871801.1:p.Ser1422Arg
NM_001288989.2:c.5188A>C NP_001275918.1:p.Ser1730Arg
NM_016341.4:c.5236A>C MANE Select NP_057425.3:p.Ser1746Arg
ENST00000260766.7:c.5236A>C ENSP00000260766.3:p.Ser1746Arg
ENST00000371375.1:n.4312A>C ENSP00000360426.1:p.Ser1438Arg
ENST00000371380.7:c.5236A>C ENSP00000360431.2:p.Ser1746Arg
ENST00000371385.7:c.4312A>C ENSP00000360438.3:p.Ser1438Arg