Canonical Allele Identifier: CA377642062
Gene: PLCE1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94298573T>A , CM000672.2:g.94298573T>A GRCh38
NC_000010.10:g.96058330T>A , CM000672.1:g.96058330T>A GRCh37
NC_000010.9:g.96048320T>A NCBI36
NG_015799.1:g.309585T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371375.2:n.4438T>A ENSP00000360426.1:p.Tyr1480Asn
ENST00000685253.1:c.*1905T>A ENSP00000509405.1:n.*1905T>A
ENST00000685889.1:n.2097T>A
ENST00000686807.1:n.781T>A
ENST00000686954.1:c.*646T>A ENSP00000508416.1:n.*646T>A
ENST00000688810.1:n.4390T>A ENSP00000509140.1:p.Tyr1464Asn
ENST00000689233.1:n.9570T>A
ENST00000690340.1:n.3035T>A
ENST00000692286.1:c.5230T>A ENSP00000509490.1:p.Tyr1744Asn
ENST00000692396.1:c.5314T>A ENSP00000508605.1:p.Tyr1772Asn
ENST00000371380.8:c.5362T>A MANE Select ENSP00000360431.2:p.Tyr1788Asn
ENST00000371385.8:c.4336T>A ENSP00000360438.4:p.Tyr1446Asn
ENST00000674738.1:n.3917T>A
ENST00000674827.1:n.3478T>A ENSP00000502523.1:p.Tyr1160Asn
ENST00000675218.1:n.4438T>A ENSP00000501910.1:p.Tyr1480Asn
ENST00000675487.1:c.*1295T>A ENSP00000502340.1:n.*1295T>A
ENST00000675718.1:n.4631T>A
ENST00000260766.7:c.5362T>A ENSP00000260766.3:p.Tyr1788Asn
ENST00000371375.1:n.4438T>A ENSP00000360426.1:p.Tyr1480Asn
ENST00000371380.7:c.5362T>A ENSP00000360431.2:p.Tyr1788Asn
ENST00000371385.7:c.4438T>A ENSP00000360438.3:p.Tyr1480Asn
NM_001165979.2:c.4438T>A NP_001159451.1:p.Tyr1480Asn
NM_001288989.1:c.5314T>A NP_001275918.1:p.Tyr1772Asn
NM_016341.3:c.5362T>A NP_057425.3:p.Tyr1788Asn
XM_006717885.2:c.5404T>A XP_006717948.1:p.Tyr1802Asn
XM_006717886.2:c.5404T>A XP_006717949.1:p.Tyr1802Asn
XM_006717888.2:c.5401T>A XP_006717951.1:p.Tyr1801Asn
XM_006717889.2:c.5356T>A XP_006717952.1:p.Tyr1786Asn
XM_006717890.1:c.4480T>A XP_006717953.1:p.Tyr1494Asn
XM_011539849.1:c.5404T>A XP_011538151.1:p.Tyr1802Asn
XM_011539850.1:c.4249T>A XP_011538152.1:p.Tyr1417Asn
XM_006717885.4:c.5404T>A XP_006717948.1:p.Tyr1802Asn
XM_006717888.4:c.5401T>A XP_006717951.1:p.Tyr1801Asn
XM_006717889.4:c.5356T>A XP_006717952.1:p.Tyr1786Asn
XM_006717890.3:c.4480T>A XP_006717953.1:p.Tyr1494Asn
XM_011539849.3:c.5404T>A XP_011538151.1:p.Tyr1802Asn
XM_011539850.3:c.4249T>A XP_011538152.1:p.Tyr1417Asn
XM_017016310.2:c.5404T>A XP_016871799.1:p.Tyr1802Asn
XM_017016311.2:c.5404T>A XP_016871800.1:p.Tyr1802Asn
XM_017016312.2:c.4390T>A XP_016871801.1:p.Tyr1464Asn
NM_001288989.2:c.5314T>A NP_001275918.1:p.Tyr1772Asn
NM_016341.4:c.5362T>A MANE Select NP_057425.3:p.Tyr1788Asn