Canonical Allele Identifier: CA1928998404

Gene: PLCE1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298464T= , CM000672.2:g.94298464T=	GRCh38
NC_000010.10:g.96058221T= , CM000672.1:g.96058221T=	GRCh37
NC_000010.9:g.96048211T=	NCBI36
NG_015799.1:g.309476T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000371375.2:c.4329T=	ENSP00000360426.1:p.Thr1443=
ENST00000685253.1:c.*1796T=	ENSP00000509405.1:n.*1796T=
ENST00000685889.1:n.1988T=
ENST00000686807.1:n.672T=
ENST00000686954.1:c.*537T=	ENSP00000508416.1:n.*537T=
ENST00000688810.1:c.4281T=	ENSP00000509140.1:p.Thr1427=
ENST00000689233.1:n.9461T=
ENST00000690340.1:n.2926T=
ENST00000692286.1:c.5121T=	ENSP00000509490.1:p.Thr1707=
ENST00000692396.1:c.5205T=	ENSP00000508605.1:p.Thr1735=
ENST00000371380.8:c.5253T= MANE Select	ENSP00000360431.2:p.Thr1751=
ENST00000371385.8:c.4227T=	ENSP00000360438.4:p.Thr1409=
ENST00000674738.1:c.3808T=
ENST00000674827.1:c.3369T=	ENSP00000502523.1:p.Thr1123=
ENST00000675218.1:c.4329T=	ENSP00000501910.1:p.Thr1443=
ENST00000675487.1:c.*1186T=	ENSP00000502340.1:n.*1186T=
ENST00000675718.1:c.4522T=
ENST00000676102.1:c.4098T=	ENSP00000502811.1:p.Thr1366=
ENST00000260766.7:c.5253T=	ENSP00000260766.3:p.Thr1751=
ENST00000371375.1:c.4329T=	ENSP00000360426.1:p.Thr1443=
ENST00000371380.7:c.5253T=	ENSP00000360431.2:p.Thr1751=
ENST00000371385.7:c.4329T=	ENSP00000360438.3:p.Thr1443=
NM_001165979.2:c.4329T=	NP_001159451.1:p.Thr1443=
NM_001288989.1:c.5205T=	NP_001275918.1:p.Thr1735=
NM_016341.3:c.5253T=	NP_057425.3:p.Thr1751=
XM_006717885.2:c.5295T=	XP_006717948.1:p.Thr1765=
XM_006717886.2:c.5295T=	XP_006717949.1:p.Thr1765=
XM_006717888.2:c.5292T=	XP_006717951.1:p.Thr1764=
XM_006717889.2:c.5247T=	XP_006717952.1:p.Thr1749=
XM_006717890.1:c.4371T=	XP_006717953.1:p.Thr1457=
XM_011539849.1:c.5295T=	XP_011538151.1:p.Thr1765=
XM_011539850.1:c.4140T=	XP_011538152.1:p.Thr1380=
XM_006717885.4:c.5295T=	XP_006717948.1:p.Thr1765=
XM_006717888.4:c.5292T=	XP_006717951.1:p.Thr1764=
XM_006717889.4:c.5247T=	XP_006717952.1:p.Thr1749=
XM_006717890.3:c.4371T=	XP_006717953.1:p.Thr1457=
XM_011539849.3:c.5295T=	XP_011538151.1:p.Thr1765=
XM_011539850.3:c.4140T=	XP_011538152.1:p.Thr1380=
XM_017016310.2:c.5295T=	XP_016871799.1:p.Thr1765=
XM_017016311.2:c.5295T=	XP_016871800.1:p.Thr1765=
XM_017016312.2:c.4281T=	XP_016871801.1:p.Thr1427=
NM_001288989.2:c.5205T=	NP_001275918.1:p.Thr1735=
NM_016341.4:c.5253T= MANE Select	NP_057425.3:p.Thr1751=