Canonical Allele Identifier: CA377641799
Gene: PLCE1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94298450G>T , CM000672.2:g.94298450G>T GRCh38
NC_000010.10:g.96058207G>T , CM000672.1:g.96058207G>T GRCh37
NC_000010.9:g.96048197G>T NCBI36
NG_015799.1:g.309462G>T

Transcript Alleles

HGVS Amino-acid change
NM_001165979.2:c.4315G>T NP_001159451.1:p.Ala1439Ser
NM_001288989.1:c.5191G>T NP_001275918.1:p.Ala1731Ser
NM_016341.3:c.5239G>T NP_057425.3:p.Ala1747Ser
XM_006717885.2:c.5281G>T XP_006717948.1:p.Ala1761Ser
XM_006717886.2:c.5281G>T XP_006717949.1:p.Ala1761Ser
XM_006717888.2:c.5278G>T XP_006717951.1:p.Ala1760Ser
XM_006717889.2:c.5233G>T XP_006717952.1:p.Ala1745Ser
XM_006717890.1:c.4357G>T XP_006717953.1:p.Ala1453Ser
XM_011539849.1:c.5281G>T XP_011538151.1:p.Ala1761Ser
XM_011539850.1:c.4126G>T XP_011538152.1:p.Ala1376Ser
XM_006717885.4:c.5281G>T XP_006717948.1:p.Ala1761Ser
XM_006717888.4:c.5278G>T XP_006717951.1:p.Ala1760Ser
XM_006717889.4:c.5233G>T XP_006717952.1:p.Ala1745Ser
XM_006717890.3:c.4357G>T XP_006717953.1:p.Ala1453Ser
XM_011539849.3:c.5281G>T XP_011538151.1:p.Ala1761Ser
XM_011539850.3:c.4126G>T XP_011538152.1:p.Ala1376Ser
XM_017016310.2:c.5281G>T XP_016871799.1:p.Ala1761Ser
XM_017016311.2:c.5281G>T XP_016871800.1:p.Ala1761Ser
XM_017016312.2:c.4267G>T XP_016871801.1:p.Ala1423Ser
NM_001288989.2:c.5191G>T NP_001275918.1:p.Ala1731Ser
NM_016341.4:c.5239G>T MANE Select NP_057425.3:p.Ala1747Ser
ENST00000260766.7:c.5239G>T ENSP00000260766.3:p.Ala1747Ser
ENST00000371375.1:n.4315G>T ENSP00000360426.1:p.Ala1439Ser
ENST00000371380.7:c.5239G>T ENSP00000360431.2:p.Ala1747Ser
ENST00000371385.7:c.4315G>T ENSP00000360438.3:p.Ala1439Ser