Canonical Allele Identifier: CA377641794
Gene: PLCE1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94298448G>C , CM000672.2:g.94298448G>C GRCh38
NC_000010.10:g.96058205G>C , CM000672.1:g.96058205G>C GRCh37
NC_000010.9:g.96048195G>C NCBI36
NG_015799.1:g.309460G>C

Transcript Alleles

HGVS Amino-acid change
NM_001165979.2:c.4313G>C NP_001159451.1:p.Ser1438Thr
NM_001288989.1:c.5189G>C NP_001275918.1:p.Ser1730Thr
NM_016341.3:c.5237G>C NP_057425.3:p.Ser1746Thr
XM_006717885.2:c.5279G>C XP_006717948.1:p.Ser1760Thr
XM_006717886.2:c.5279G>C XP_006717949.1:p.Ser1760Thr
XM_006717888.2:c.5276G>C XP_006717951.1:p.Ser1759Thr
XM_006717889.2:c.5231G>C XP_006717952.1:p.Ser1744Thr
XM_006717890.1:c.4355G>C XP_006717953.1:p.Ser1452Thr
XM_011539849.1:c.5279G>C XP_011538151.1:p.Ser1760Thr
XM_011539850.1:c.4124G>C XP_011538152.1:p.Ser1375Thr
XM_006717885.4:c.5279G>C XP_006717948.1:p.Ser1760Thr
XM_006717888.4:c.5276G>C XP_006717951.1:p.Ser1759Thr
XM_006717889.4:c.5231G>C XP_006717952.1:p.Ser1744Thr
XM_006717890.3:c.4355G>C XP_006717953.1:p.Ser1452Thr
XM_011539849.3:c.5279G>C XP_011538151.1:p.Ser1760Thr
XM_011539850.3:c.4124G>C XP_011538152.1:p.Ser1375Thr
XM_017016310.2:c.5279G>C XP_016871799.1:p.Ser1760Thr
XM_017016311.2:c.5279G>C XP_016871800.1:p.Ser1760Thr
XM_017016312.2:c.4265G>C XP_016871801.1:p.Ser1422Thr
NM_001288989.2:c.5189G>C NP_001275918.1:p.Ser1730Thr
NM_016341.4:c.5237G>C MANE Select NP_057425.3:p.Ser1746Thr
ENST00000260766.7:c.5237G>C ENSP00000260766.3:p.Ser1746Thr
ENST00000371375.1:n.4313G>C ENSP00000360426.1:p.Ser1438Thr
ENST00000371380.7:c.5237G>C ENSP00000360431.2:p.Ser1746Thr
ENST00000371385.7:c.4313G>C ENSP00000360438.3:p.Ser1438Thr