Canonical Allele Identifier: CA377642061
Gene: PLCE1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94298571C>G , CM000672.2:g.94298571C>G GRCh38
NC_000010.10:g.96058328C>G , CM000672.1:g.96058328C>G GRCh37
NC_000010.9:g.96048318C>G NCBI36
NG_015799.1:g.309583C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371375.2:n.4436C>G ENSP00000360426.1:p.Thr1479Ser
ENST00000685253.1:c.*1903C>G ENSP00000509405.1:n.*1903C>G
ENST00000685889.1:n.2095C>G
ENST00000686807.1:n.779C>G
ENST00000686954.1:c.*644C>G ENSP00000508416.1:n.*644C>G
ENST00000688810.1:n.4388C>G ENSP00000509140.1:p.Thr1463Ser
ENST00000689233.1:n.9568C>G
ENST00000690340.1:n.3033C>G
ENST00000692286.1:c.5228C>G ENSP00000509490.1:p.Thr1743Ser
ENST00000692396.1:c.5312C>G ENSP00000508605.1:p.Thr1771Ser
ENST00000371380.8:c.5360C>G MANE Select ENSP00000360431.2:p.Thr1787Ser
ENST00000371385.8:c.4334C>G ENSP00000360438.4:p.Thr1445Ser
ENST00000674738.1:n.3915C>G
ENST00000674827.1:n.3476C>G ENSP00000502523.1:p.Thr1159Ser
ENST00000675218.1:n.4436C>G ENSP00000501910.1:p.Thr1479Ser
ENST00000675487.1:c.*1293C>G ENSP00000502340.1:n.*1293C>G
ENST00000675718.1:n.4629C>G
ENST00000260766.7:c.5360C>G ENSP00000260766.3:p.Thr1787Ser
ENST00000371375.1:n.4436C>G ENSP00000360426.1:p.Thr1479Ser
ENST00000371380.7:c.5360C>G ENSP00000360431.2:p.Thr1787Ser
ENST00000371385.7:c.4436C>G ENSP00000360438.3:p.Thr1479Ser
NM_001165979.2:c.4436C>G NP_001159451.1:p.Thr1479Ser
NM_001288989.1:c.5312C>G NP_001275918.1:p.Thr1771Ser
NM_016341.3:c.5360C>G NP_057425.3:p.Thr1787Ser
XM_006717885.2:c.5402C>G XP_006717948.1:p.Thr1801Ser
XM_006717886.2:c.5402C>G XP_006717949.1:p.Thr1801Ser
XM_006717888.2:c.5399C>G XP_006717951.1:p.Thr1800Ser
XM_006717889.2:c.5354C>G XP_006717952.1:p.Thr1785Ser
XM_006717890.1:c.4478C>G XP_006717953.1:p.Thr1493Ser
XM_011539849.1:c.5402C>G XP_011538151.1:p.Thr1801Ser
XM_011539850.1:c.4247C>G XP_011538152.1:p.Thr1416Ser
XM_006717885.4:c.5402C>G XP_006717948.1:p.Thr1801Ser
XM_006717888.4:c.5399C>G XP_006717951.1:p.Thr1800Ser
XM_006717889.4:c.5354C>G XP_006717952.1:p.Thr1785Ser
XM_006717890.3:c.4478C>G XP_006717953.1:p.Thr1493Ser
XM_011539849.3:c.5402C>G XP_011538151.1:p.Thr1801Ser
XM_011539850.3:c.4247C>G XP_011538152.1:p.Thr1416Ser
XM_017016310.2:c.5402C>G XP_016871799.1:p.Thr1801Ser
XM_017016311.2:c.5402C>G XP_016871800.1:p.Thr1801Ser
XM_017016312.2:c.4388C>G XP_016871801.1:p.Thr1463Ser
NM_001288989.2:c.5312C>G NP_001275918.1:p.Thr1771Ser
NM_016341.4:c.5360C>G MANE Select NP_057425.3:p.Thr1787Ser