Canonical Allele Identifier: CA470986555
Gene: PLCE1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96058302G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94298545G>A , CM000672.2:g.94298545G>A GRCh38
NC_000010.10:g.96058302G>A , CM000672.1:g.96058302G>A GRCh37
NC_000010.9:g.96048292G>A NCBI36
NG_015799.1:g.309557G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371380.8:c.5334G>A MANE Select ENSP00000360431.2:p.Gln1778=
ENST00000371385.8:c.4308G>A ENSP00000360438.4:p.Gln1436=
ENST00000674738.1:n.3889G>A
ENST00000674827.1:n.3450G>A ENSP00000502523.1:p.Gln1150=
ENST00000675218.1:n.4410G>A ENSP00000501910.1:p.Gln1470=
ENST00000675487.1:c.*1267G>A ENSP00000502340.1:p.=
ENST00000675718.1:n.4603G>A
ENST00000260766.7:c.5334G>A ENSP00000260766.3:p.Gln1778=
ENST00000371375.1:n.4410G>A ENSP00000360426.1:p.Gln1470=
ENST00000371380.7:c.5334G>A ENSP00000360431.2:p.Gln1778=
ENST00000371385.7:c.4410G>A ENSP00000360438.3:p.Gln1470=
NM_001165979.2:c.4410G>A NP_001159451.1:p.Gln1470=
NM_001288989.1:c.5286G>A NP_001275918.1:p.Gln1762=
NM_016341.3:c.5334G>A NP_057425.3:p.Gln1778=
XM_006717885.2:c.5376G>A XP_006717948.1:p.Gln1792=
XM_006717886.2:c.5376G>A XP_006717949.1:p.Gln1792=
XM_006717888.2:c.5373G>A XP_006717951.1:p.Gln1791=
XM_006717889.2:c.5328G>A XP_006717952.1:p.Gln1776=
XM_006717890.1:c.4452G>A XP_006717953.1:p.Gln1484=
XM_011539849.1:c.5376G>A XP_011538151.1:p.Gln1792=
XM_011539850.1:c.4221G>A XP_011538152.1:p.Gln1407=
XM_006717885.4:c.5376G>A XP_006717948.1:p.Gln1792=
XM_006717888.4:c.5373G>A XP_006717951.1:p.Gln1791=
XM_006717889.4:c.5328G>A XP_006717952.1:p.Gln1776=
XM_006717890.3:c.4452G>A XP_006717953.1:p.Gln1484=
XM_011539849.3:c.5376G>A XP_011538151.1:p.Gln1792=
XM_011539850.3:c.4221G>A XP_011538152.1:p.Gln1407=
XM_017016310.2:c.5376G>A XP_016871799.1:p.Gln1792=
XM_017016311.2:c.5376G>A XP_016871800.1:p.Gln1792=
XM_017016312.2:c.4362G>A XP_016871801.1:p.Gln1454=
NM_001288989.2:c.5286G>A NP_001275918.1:p.Gln1762=
NM_016341.4:c.5334G>A MANE Select NP_057425.3:p.Gln1778=