Canonical Allele Identifier: CA470986588
Gene: PLCE1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96058335T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94298578T>G , CM000672.2:g.94298578T>G GRCh38
NC_000010.10:g.96058335T>G , CM000672.1:g.96058335T>G GRCh37
NC_000010.9:g.96048325T>G NCBI36
NG_015799.1:g.309590T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371375.2:c.4443T>G ENSP00000360426.1:p.Pro1481=
ENST00000685253.1:c.*1910T>G ENSP00000509405.1:n.*1910T>G
ENST00000685889.1:n.2102T>G
ENST00000686807.1:n.786T>G
ENST00000686954.1:c.*651T>G ENSP00000508416.1:n.*651T>G
ENST00000688810.1:c.4395T>G ENSP00000509140.1:p.Pro1465=
ENST00000689233.1:n.9575T>G
ENST00000690340.1:n.3040T>G
ENST00000692286.1:c.5235T>G ENSP00000509490.1:p.Pro1745=
ENST00000692396.1:c.5319T>G ENSP00000508605.1:p.Pro1773=
ENST00000371380.8:c.5367T>G MANE Select ENSP00000360431.2:p.Pro1789=
ENST00000371385.8:c.4341T>G ENSP00000360438.4:p.Pro1447=
ENST00000674738.1:c.3922T>G
ENST00000674827.1:c.3483T>G ENSP00000502523.1:p.Pro1161=
ENST00000675218.1:c.4443T>G ENSP00000501910.1:p.Pro1481=
ENST00000675487.1:c.*1300T>G ENSP00000502340.1:n.*1300T>G
ENST00000675718.1:c.4636T>G
ENST00000260766.7:c.5367T>G ENSP00000260766.3:p.Pro1789=
ENST00000371375.1:c.4443T>G ENSP00000360426.1:p.Pro1481=
ENST00000371380.7:c.5367T>G ENSP00000360431.2:p.Pro1789=
ENST00000371385.7:c.4443T>G ENSP00000360438.3:p.Pro1481=
NM_001165979.2:c.4443T>G NP_001159451.1:p.Pro1481=
NM_001288989.1:c.5319T>G NP_001275918.1:p.Pro1773=
NM_016341.3:c.5367T>G NP_057425.3:p.Pro1789=
XM_006717885.2:c.5409T>G XP_006717948.1:p.Pro1803=
XM_006717886.2:c.5409T>G XP_006717949.1:p.Pro1803=
XM_006717888.2:c.5406T>G XP_006717951.1:p.Pro1802=
XM_006717889.2:c.5361T>G XP_006717952.1:p.Pro1787=
XM_006717890.1:c.4485T>G XP_006717953.1:p.Pro1495=
XM_011539849.1:c.5409T>G XP_011538151.1:p.Pro1803=
XM_011539850.1:c.4254T>G XP_011538152.1:p.Pro1418=
XM_006717885.4:c.5409T>G XP_006717948.1:p.Pro1803=
XM_006717888.4:c.5406T>G XP_006717951.1:p.Pro1802=
XM_006717889.4:c.5361T>G XP_006717952.1:p.Pro1787=
XM_006717890.3:c.4485T>G XP_006717953.1:p.Pro1495=
XM_011539849.3:c.5409T>G XP_011538151.1:p.Pro1803=
XM_011539850.3:c.4254T>G XP_011538152.1:p.Pro1418=
XM_017016310.2:c.5409T>G XP_016871799.1:p.Pro1803=
XM_017016311.2:c.5409T>G XP_016871800.1:p.Pro1803=
XM_017016312.2:c.4395T>G XP_016871801.1:p.Pro1465=
NM_001288989.2:c.5319T>G NP_001275918.1:p.Pro1773=
NM_016341.4:c.5367T>G MANE Select NP_057425.3:p.Pro1789=