Canonical Allele Identifier: CA2846633666
Gene: PLCE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94298683_94298684insCCCGAAAGGG , CM000672.2:g.94298683_94298684insCCCGAAAGGG GRCh38
NC_000010.10:g.96058440_96058441insCCCGAAAGGG , CM000672.1:g.96058440_96058441insCCCGAAAGGG GRCh37
NC_000010.9:g.96048430_96048431insCCCGAAAGGG NCBI36
NG_015799.1:g.309695_309696insCCCGAAAGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000371375.2:c.4534+14_4534+15insCCCGAAAGGG ENSP00000360426.1:n.4534+14_4534+15insCCCGAAAGGG
ENST00000685253.1:c.*2001+14_*2001+15insCCCGAAAGGG ENSP00000509405.1:n.*2001+14_*2001+15insCCCGAAAGGG
ENST00000685889.1:n.2193+14_2193+15insCCCGAAAGGG
ENST00000686807.1:n.877+14_877+15insCCCGAAAGGG
ENST00000686954.1:c.*742+14_*742+15insCCCGAAAGGG ENSP00000508416.1:n.*742+14_*742+15insCCCGAAAGGG
ENST00000688810.1:c.4486+14_4486+15insCCCGAAAGGG ENSP00000509140.1:n.4486+14_4486+15insCCCGAAAGGG
ENST00000689233.1:n.9666+14_9666+15insCCCGAAAGGG
ENST00000690340.1:n.3131+14_3131+15insCCCGAAAGGG
ENST00000692286.1:c.5326+14_5326+15insCCCGAAAGGG ENSP00000509490.1:n.5326+14_5326+15insCCCGAAAGGG
ENST00000692396.1:c.5410+14_5410+15insCCCGAAAGGG ENSP00000508605.1:n.5410+14_5410+15insCCCGAAAGGG
ENST00000371380.8:c.5458+14_5458+15insCCCGAAAGGG MANE Select ENSP00000360431.2:n.5458+14_5458+15insCCCGAAAGGG
ENST00000371385.8:c.4432+14_4432+15insCCCGAAAGGG ENSP00000360438.4:n.4432+14_4432+15insCCCGAAAGGG
ENST00000674738.1:c.4013+14_4013+15insCCCGAAAGGG
ENST00000674827.1:c.3574+14_3574+15insCCCGAAAGGG ENSP00000502523.1:n.3574+14_3574+15insCCCGAAAGGG
ENST00000675218.1:c.4534+14_4534+15insCCCGAAAGGG ENSP00000501910.1:n.4534+14_4534+15insCCCGAAAGGG
ENST00000675487.1:c.*1391+14_*1391+15insCCCGAAAGGG ENSP00000502340.1:n.*1391+14_*1391+15insCCCGAAAGGG
ENST00000675718.1:c.4727+14_4727+15insCCCGAAAGGG
ENST00000260766.7:c.5458+14_5458+15insCCCGAAAGGG ENSP00000260766.3:n.5458+14_5458+15insCCCGAAAGGG
ENST00000371375.1:c.4534+14_4534+15insCCCGAAAGGG ENSP00000360426.1:n.4534+14_4534+15insCCCGAAAGGG
ENST00000371380.7:c.5458+14_5458+15insCCCGAAAGGG ENSP00000360431.2:n.5458+14_5458+15insCCCGAAAGGG
ENST00000371385.7:c.4534+14_4534+15insCCCGAAAGGG ENSP00000360438.3:n.4534+14_4534+15insCCCGAAAGGG
NM_001165979.2:c.4534+14_4534+15insCCCGAAAGGG NP_001159451.1:n.4534+14_4534+15insCCCGAAAGGG
NM_001288989.1:c.5410+14_5410+15insCCCGAAAGGG NP_001275918.1:n.5410+14_5410+15insCCCGAAAGGG
NM_016341.3:c.5458+14_5458+15insCCCGAAAGGG NP_057425.3:n.5458+14_5458+15insCCCGAAAGGG
XM_006717885.2:c.5500+14_5500+15insCCCGAAAGGG XP_006717948.1:n.5500+14_5500+15insCCCGAAAGGG
XM_006717886.2:c.5500+14_5500+15insCCCGAAAGGG XP_006717949.1:n.5500+14_5500+15insCCCGAAAGGG
XM_006717888.2:c.5497+14_5497+15insCCCGAAAGGG XP_006717951.1:n.5497+14_5497+15insCCCGAAAGGG
XM_006717889.2:c.5452+14_5452+15insCCCGAAAGGG XP_006717952.1:n.5452+14_5452+15insCCCGAAAGGG
XM_006717890.1:c.4576+14_4576+15insCCCGAAAGGG XP_006717953.1:n.4576+14_4576+15insCCCGAAAGGG
XM_011539849.1:c.5500+14_5500+15insCCCGAAAGGG XP_011538151.1:n.5500+14_5500+15insCCCGAAAGGG
XM_011539850.1:c.4345+14_4345+15insCCCGAAAGGG XP_011538152.1:n.4345+14_4345+15insCCCGAAAGGG
XM_006717885.4:c.5500+14_5500+15insCCCGAAAGGG XP_006717948.1:n.5500+14_5500+15insCCCGAAAGGG
XM_006717888.4:c.5497+14_5497+15insCCCGAAAGGG XP_006717951.1:n.5497+14_5497+15insCCCGAAAGGG
XM_006717889.4:c.5452+14_5452+15insCCCGAAAGGG XP_006717952.1:n.5452+14_5452+15insCCCGAAAGGG
XM_006717890.3:c.4576+14_4576+15insCCCGAAAGGG XP_006717953.1:n.4576+14_4576+15insCCCGAAAGGG
XM_011539849.3:c.5500+14_5500+15insCCCGAAAGGG XP_011538151.1:n.5500+14_5500+15insCCCGAAAGGG
XM_011539850.3:c.4345+14_4345+15insCCCGAAAGGG XP_011538152.1:n.4345+14_4345+15insCCCGAAAGGG
XM_017016310.2:c.5500+14_5500+15insCCCGAAAGGG XP_016871799.1:n.5500+14_5500+15insCCCGAAAGGG
XM_017016311.2:c.5500+14_5500+15insCCCGAAAGGG XP_016871800.1:n.5500+14_5500+15insCCCGAAAGGG
XM_017016312.2:c.4486+14_4486+15insCCCGAAAGGG XP_016871801.1:n.4486+14_4486+15insCCCGAAAGGG
NM_001288989.2:c.5410+14_5410+15insCCCGAAAGGG NP_001275918.1:n.5410+14_5410+15insCCCGAAAGGG
NM_016341.4:c.5458+14_5458+15insCCCGAAAGGG MANE Select NP_057425.3:n.5458+14_5458+15insCCCGAAAGGG