Canonical Allele Identifier: CA931353182
Gene: PLCE1 HGNC NCBI

Linked Data

dbSNP Id: rs2052712614

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94293648_94293650dup , CM000672.2:g.94293648_94293650dup GRCh38
NC_000010.10:g.96053405_96053407dup , CM000672.1:g.96053405_96053407dup GRCh37
NC_000010.9:g.96043395_96043397dup NCBI36
NG_015799.1:g.304660_304662dup

Transcript Alleles

HGVS Amino-acid change
ENST00000371375.2:c.4243+9_4243+11dup ENSP00000360426.1:n.4243+9_4243+11dup
ENST00000685253.1:c.*1710+9_*1710+11dup ENSP00000509405.1:n.*1710+9_*1710+11dup
ENST00000685889.1:n.1902+9_1902+11dup
ENST00000686807.1:n.586+9_586+11dup
ENST00000686954.1:c.*451+9_*451+11dup ENSP00000508416.1:n.*451+9_*451+11dup
ENST00000688810.1:c.4195+9_4195+11dup ENSP00000509140.1:n.4195+9_4195+11dup
ENST00000689233.1:n.9375+9_9375+11dup
ENST00000690340.1:n.2840+9_2840+11dup
ENST00000692286.1:c.5036-4731_5036-4729dup ENSP00000509490.1:n.5036-4731_5036-4729du...
ENST00000692396.1:c.5119+9_5119+11dup ENSP00000508605.1:n.5119+9_5119+11dup
ENST00000371380.8:c.5167+9_5167+11dup MANE Select ENSP00000360431.2:n.5167+9_5167+11dup
ENST00000371385.8:c.4141+9_4141+11dup ENSP00000360438.4:n.4141+9_4141+11dup
ENST00000674738.1:c.3722+9_3722+11dup
ENST00000674827.1:c.3283+9_3283+11dup ENSP00000502523.1:n.3283+9_3283+11dup
ENST00000675218.1:c.4243+9_4243+11dup ENSP00000501910.1:n.4243+9_4243+11dup
ENST00000675487.1:c.*1100+9_*1100+11dup ENSP00000502340.1:n.*1100+9_*1100+11dup
ENST00000675718.1:c.4436+9_4436+11dup
ENST00000676102.1:c.4012+9_4012+11dup ENSP00000502811.1:n.4012+9_4012+11dup
ENST00000260766.7:c.5167+9_5167+11dup ENSP00000260766.3:n.5167+9_5167+11dup
ENST00000371375.1:c.4243+9_4243+11dup ENSP00000360426.1:n.4243+9_4243+11dup
ENST00000371380.7:c.5167+9_5167+11dup ENSP00000360431.2:n.5167+9_5167+11dup
ENST00000371385.7:c.4243+9_4243+11dup ENSP00000360438.3:n.4243+9_4243+11dup
NM_001165979.2:c.4243+9_4243+11dup NP_001159451.1:n.4243+9_4243+11dup
NM_001288989.1:c.5119+9_5119+11dup NP_001275918.1:n.5119+9_5119+11dup
NM_016341.3:c.5167+9_5167+11dup NP_057425.3:n.5167+9_5167+11dup
XM_006717885.2:c.5209+9_5209+11dup XP_006717948.1:n.5209+9_5209+11dup
XM_006717886.2:c.5209+9_5209+11dup XP_006717949.1:n.5209+9_5209+11dup
XM_006717888.2:c.5206+9_5206+11dup XP_006717951.1:n.5206+9_5206+11dup
XM_006717889.2:c.5161+9_5161+11dup XP_006717952.1:n.5161+9_5161+11dup
XM_006717890.1:c.4285+9_4285+11dup XP_006717953.1:n.4285+9_4285+11dup
XM_011539849.1:c.5209+9_5209+11dup XP_011538151.1:n.5209+9_5209+11dup
XM_011539850.1:c.4054+9_4054+11dup XP_011538152.1:n.4054+9_4054+11dup
XM_006717885.4:c.5209+9_5209+11dup XP_006717948.1:n.5209+9_5209+11dup
XM_006717888.4:c.5206+9_5206+11dup XP_006717951.1:n.5206+9_5206+11dup
XM_006717889.4:c.5161+9_5161+11dup XP_006717952.1:n.5161+9_5161+11dup
XM_006717890.3:c.4285+9_4285+11dup XP_006717953.1:n.4285+9_4285+11dup
XM_011539849.3:c.5209+9_5209+11dup XP_011538151.1:n.5209+9_5209+11dup
XM_011539850.3:c.4054+9_4054+11dup XP_011538152.1:n.4054+9_4054+11dup
XM_017016310.2:c.5209+9_5209+11dup XP_016871799.1:n.5209+9_5209+11dup
XM_017016311.2:c.5209+9_5209+11dup XP_016871800.1:n.5209+9_5209+11dup
XM_017016312.2:c.4195+9_4195+11dup XP_016871801.1:n.4195+9_4195+11dup
NM_001288989.2:c.5119+9_5119+11dup NP_001275918.1:n.5119+9_5119+11dup
NM_016341.4:c.5167+9_5167+11dup MANE Select NP_057425.3:n.5167+9_5167+11dup