Canonical Allele Identifier: CA1929017180

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94322116A= , CM000672.2:g.94322116A= GRCh38
NC_000010.10:g.96081873A= , CM000672.1:g.96081873A= GRCh37
NC_000010.9:g.96071863A= NCBI36
NG_015799.1:g.333128A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371375.2:c.5577+57A= (PLCE1) ENSP00000360426.1:n.5577+57A=
ENST00000685253.1:c.*3044+57A= (PLCE1) ENSP00000509405.1:n.*3044+57A=
ENST00000685889.1:n.3236+57A= (PLCE1)
ENST00000686807.1:n.1920+57A= (PLCE1)
ENST00000686954.1:c.*1785+57A= (PLCE1) ENSP00000508416.1:n.*1785+57A=
ENST00000688810.1:c.5529+57A= (PLCE1) ENSP00000509140.1:n.5529+57A=
ENST00000689233.1:n.10709+57A= (PLCE1)
ENST00000690340.1:n.4174+57A= (PLCE1)
ENST00000692286.1:c.6369+57A= (PLCE1) ENSP00000509490.1:n.6369+57A=
ENST00000692396.1:c.6453+57A= (PLCE1) ENSP00000508605.1:n.6453+57A=
ENST00000371380.8:c.6501+57A= (PLCE1) MANE Select ENSP00000360431.2:n.6501+57A=
ENST00000371385.8:c.5475+57A= (PLCE1) ENSP00000360438.4:n.5475+57A=
ENST00000675218.1:c.5577+57A= (PLCE1) ENSP00000501910.1:n.5577+57A=
ENST00000675487.1:c.*2434+57A= (PLCE1) ENSP00000502340.1:n.*2434+57A=
ENST00000260766.7:c.6501+57A= (PLCE1) ENSP00000260766.3:n.6501+57A=
ENST00000371375.1:c.5577+57A= (PLCE1) ENSP00000360426.1:n.5577+57A=
ENST00000371380.7:c.6501+57A= (PLCE1) ENSP00000360431.2:n.6501+57A=
ENST00000371385.7:c.5577+57A= (PLCE1) ENSP00000360438.3:n.5577+57A=
NM_001165979.2:c.5577+57A= (PLCE1) NP_001159451.1:n.5577+57A=
NM_001288989.1:c.6453+57A= (PLCE1) NP_001275918.1:n.6453+57A=
NM_016341.3:c.6501+57A= (PLCE1) NP_057425.3:n.6501+57A=
XM_006717885.2:c.6543+57A= (PLCE1) XP_006717948.1:n.6543+57A=
XM_006717886.2:c.6543+57A= (PLCE1) XP_006717949.1:n.6543+57A=
XM_006717888.2:c.6540+57A= (PLCE1) XP_006717951.1:n.6540+57A=
XM_006717889.2:c.6495+57A= (PLCE1) XP_006717952.1:n.6495+57A=
XM_006717890.1:c.5619+57A= (PLCE1) XP_006717953.1:n.5619+57A=
XM_011539849.1:c.6543+57A= (PLCE1) XP_011538151.1:n.6543+57A=
XM_011539850.1:c.5388+57A= (PLCE1) XP_011538152.1:n.5388+57A=
XR_945799.1:n.3311-6652T= (NOC3L)
XM_006717885.4:c.6543+57A= (PLCE1) XP_006717948.1:n.6543+57A=
XM_006717888.4:c.6540+57A= (PLCE1) XP_006717951.1:n.6540+57A=
XM_006717889.4:c.6495+57A= (PLCE1) XP_006717952.1:n.6495+57A=
XM_006717890.3:c.5619+57A= (PLCE1) XP_006717953.1:n.5619+57A=
XM_011539849.3:c.6543+57A= (PLCE1) XP_011538151.1:n.6543+57A=
XM_011539850.3:c.5388+57A= (PLCE1) XP_011538152.1:n.5388+57A=
XM_017016310.2:c.6543+57A= (PLCE1) XP_016871799.1:n.6543+57A=
XM_017016311.2:c.6543+57A= (PLCE1) XP_016871800.1:n.6543+57A=
XM_017016312.2:c.5529+57A= (PLCE1) XP_016871801.1:n.5529+57A=
XR_002957007.1:n.3312-6652T= (NOC3L)
NM_001288989.2:c.6453+57A= (PLCE1) NP_001275918.1:n.6453+57A=
NM_016341.4:c.6501+57A= (PLCE1) MANE Select NP_057425.3:n.6501+57A=