Canonical Allele Identifier: CA377648256

Gene: PLCE1

Linked Data

• MyVariant Identifiers: chr10:g.96030243G>T (hg19) ; chr10:g.94270486G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94270486G>T , CM000672.2:g.94270486G>T	GRCh38
NC_000010.10:g.96030243G>T , CM000672.1:g.96030243G>T	GRCh37
NC_000010.9:g.96020233G>T	NCBI36
NG_015799.1:g.281498G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.3466G>T	ENSP00000360426.1:p.Glu1156Ter
ENST00000685253.1:c.*933G>T	ENSP00000509405.1:n.*933G>T
ENST00000685889.1:n.1125G>T
ENST00000686954.1:c.4390G>T	ENSP00000508416.1:p.Glu1464Ter
ENST00000688810.1:c.3418G>T	ENSP00000509140.1:p.Glu1140Ter
ENST00000689233.1:n.4720G>T
ENST00000692286.1:c.4390G>T	ENSP00000509490.1:p.Glu1464Ter
ENST00000692396.1:c.4342G>T	ENSP00000508605.1:p.Glu1448Ter
ENST00000371380.8:c.4390G>T MANE Select	ENSP00000360431.2:p.Glu1464Ter
ENST00000371385.8:c.3364G>T	ENSP00000360438.4:p.Glu1122Ter
ENST00000674738.1:c.2795G>T
ENST00000674827.1:c.2467G>T	ENSP00000502523.1:p.Glu823Ter
ENST00000675218.1:c.3466G>T	ENSP00000501910.1:p.Glu1156Ter
ENST00000675487.1:c.*323G>T	ENSP00000502340.1:n.*323G>T
ENST00000675718.1:c.3617G>T
ENST00000676102.1:c.3235G>T	ENSP00000502811.1:p.Glu1079Ter
ENST00000260766.7:c.4390G>T	ENSP00000260766.3:p.Glu1464Ter
ENST00000371375.1:c.3466G>T	ENSP00000360426.1:p.Glu1156Ter
ENST00000371380.7:c.4390G>T	ENSP00000360431.2:p.Glu1464Ter
ENST00000371385.7:c.3466G>T	ENSP00000360438.3:p.Glu1156Ter
NM_001165979.2:c.3466G>T	NP_001159451.1:p.Glu1156Ter
NM_001288989.1:c.4342G>T	NP_001275918.1:p.Glu1448Ter
NM_016341.3:c.4390G>T	NP_057425.3:p.Glu1464Ter
XM_006717885.2:c.4390G>T	XP_006717948.1:p.Glu1464Ter
XM_006717886.2:c.4390G>T	XP_006717949.1:p.Glu1464Ter
XM_006717888.2:c.4390G>T	XP_006717951.1:p.Glu1464Ter
XM_006717889.2:c.4342G>T	XP_006717952.1:p.Glu1448Ter
XM_006717890.1:c.3466G>T	XP_006717953.1:p.Glu1156Ter
XM_011539849.1:c.4390G>T	XP_011538151.1:p.Glu1464Ter
XM_011539850.1:c.3235G>T	XP_011538152.1:p.Glu1079Ter
XM_011539851.1:c.4390G>T	XP_011538153.1:p.Glu1464Ter
XM_011539852.1:c.4390G>T	XP_011538154.1:p.Glu1464Ter
XM_006717885.4:c.4390G>T	XP_006717948.1:p.Glu1464Ter
XM_006717888.4:c.4390G>T	XP_006717951.1:p.Glu1464Ter
XM_006717889.4:c.4342G>T	XP_006717952.1:p.Glu1448Ter
XM_006717890.3:c.3466G>T	XP_006717953.1:p.Glu1156Ter
XM_011539849.3:c.4390G>T	XP_011538151.1:p.Glu1464Ter
XM_011539850.3:c.3235G>T	XP_011538152.1:p.Glu1079Ter
XM_011539851.3:c.4390G>T	XP_011538153.1:p.Glu1464Ter
XM_011539852.3:c.4390G>T	XP_011538154.1:p.Glu1464Ter
XM_017016310.2:c.4390G>T	XP_016871799.1:p.Glu1464Ter
XM_017016311.2:c.4390G>T	XP_016871800.1:p.Glu1464Ter
XM_017016312.2:c.3418G>T	XP_016871801.1:p.Glu1140Ter
NM_001288989.2:c.4342G>T	NP_001275918.1:p.Glu1448Ter
NM_016341.4:c.4390G>T MANE Select	NP_057425.3:p.Glu1464Ter