Canonical Allele Identifier: CA377642065
Gene: PLCE1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94298574A>C , CM000672.2:g.94298574A>C GRCh38
NC_000010.10:g.96058331A>C , CM000672.1:g.96058331A>C GRCh37
NC_000010.9:g.96048321A>C NCBI36
NG_015799.1:g.309586A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000371375.2:n.4439A>C ENSP00000360426.1:p.Tyr1480Ser
ENST00000685253.1:c.*1906A>C ENSP00000509405.1:n.*1906A>C
ENST00000685889.1:n.2098A>C
ENST00000686807.1:n.782A>C
ENST00000686954.1:c.*647A>C ENSP00000508416.1:n.*647A>C
ENST00000688810.1:n.4391A>C ENSP00000509140.1:p.Tyr1464Ser
ENST00000689233.1:n.9571A>C
ENST00000690340.1:n.3036A>C
ENST00000692286.1:c.5231A>C ENSP00000509490.1:p.Tyr1744Ser
ENST00000692396.1:c.5315A>C ENSP00000508605.1:p.Tyr1772Ser
ENST00000371380.8:c.5363A>C MANE Select ENSP00000360431.2:p.Tyr1788Ser
ENST00000371385.8:c.4337A>C ENSP00000360438.4:p.Tyr1446Ser
ENST00000674738.1:n.3918A>C
ENST00000674827.1:n.3479A>C ENSP00000502523.1:p.Tyr1160Ser
ENST00000675218.1:n.4439A>C ENSP00000501910.1:p.Tyr1480Ser
ENST00000675487.1:c.*1296A>C ENSP00000502340.1:n.*1296A>C
ENST00000675718.1:n.4632A>C
ENST00000260766.7:c.5363A>C ENSP00000260766.3:p.Tyr1788Ser
ENST00000371375.1:n.4439A>C ENSP00000360426.1:p.Tyr1480Ser
ENST00000371380.7:c.5363A>C ENSP00000360431.2:p.Tyr1788Ser
ENST00000371385.7:c.4439A>C ENSP00000360438.3:p.Tyr1480Ser
NM_001165979.2:c.4439A>C NP_001159451.1:p.Tyr1480Ser
NM_001288989.1:c.5315A>C NP_001275918.1:p.Tyr1772Ser
NM_016341.3:c.5363A>C NP_057425.3:p.Tyr1788Ser
XM_006717885.2:c.5405A>C XP_006717948.1:p.Tyr1802Ser
XM_006717886.2:c.5405A>C XP_006717949.1:p.Tyr1802Ser
XM_006717888.2:c.5402A>C XP_006717951.1:p.Tyr1801Ser
XM_006717889.2:c.5357A>C XP_006717952.1:p.Tyr1786Ser
XM_006717890.1:c.4481A>C XP_006717953.1:p.Tyr1494Ser
XM_011539849.1:c.5405A>C XP_011538151.1:p.Tyr1802Ser
XM_011539850.1:c.4250A>C XP_011538152.1:p.Tyr1417Ser
XM_006717885.4:c.5405A>C XP_006717948.1:p.Tyr1802Ser
XM_006717888.4:c.5402A>C XP_006717951.1:p.Tyr1801Ser
XM_006717889.4:c.5357A>C XP_006717952.1:p.Tyr1786Ser
XM_006717890.3:c.4481A>C XP_006717953.1:p.Tyr1494Ser
XM_011539849.3:c.5405A>C XP_011538151.1:p.Tyr1802Ser
XM_011539850.3:c.4250A>C XP_011538152.1:p.Tyr1417Ser
XM_017016310.2:c.5405A>C XP_016871799.1:p.Tyr1802Ser
XM_017016311.2:c.5405A>C XP_016871800.1:p.Tyr1802Ser
XM_017016312.2:c.4391A>C XP_016871801.1:p.Tyr1464Ser
NM_001288989.2:c.5315A>C NP_001275918.1:p.Tyr1772Ser
NM_016341.4:c.5363A>C MANE Select NP_057425.3:p.Tyr1788Ser