Canonical Allele Identifier: CA470807759

Gene: PLCE1

Linked Data

• MyVariant Identifiers: chr10:g.96053386A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94293629A>T , CM000672.2:g.94293629A>T	GRCh38
NC_000010.10:g.96053386A>T , CM000672.1:g.96053386A>T	GRCh37
NC_000010.9:g.96043376A>T	NCBI36
NG_015799.1:g.304641A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.4233A>T	ENSP00000360426.1:p.Thr1411=
ENST00000685253.1:c.*1700A>T	ENSP00000509405.1:n.*1700A>T
ENST00000685889.1:n.1892A>T
ENST00000686807.1:n.576A>T
ENST00000686954.1:c.*441A>T	ENSP00000508416.1:n.*441A>T
ENST00000688810.1:c.4185A>T	ENSP00000509140.1:p.Thr1395=
ENST00000689233.1:n.9365A>T
ENST00000690340.1:n.2830A>T
ENST00000692286.1:c.5036-4750A>T	ENSP00000509490.1:n.5036-4750A>T
ENST00000692396.1:c.5109A>T	ENSP00000508605.1:p.Thr1703=
ENST00000371380.8:c.5157A>T MANE Select	ENSP00000360431.2:p.Thr1719=
ENST00000371385.8:c.4131A>T	ENSP00000360438.4:p.Thr1377=
ENST00000674738.1:c.3712A>T
ENST00000674827.1:c.3273A>T	ENSP00000502523.1:p.Thr1091=
ENST00000675218.1:c.4233A>T	ENSP00000501910.1:p.Thr1411=
ENST00000675487.1:c.*1090A>T	ENSP00000502340.1:n.*1090A>T
ENST00000675718.1:c.4426A>T
ENST00000676102.1:c.4002A>T	ENSP00000502811.1:p.Thr1334=
ENST00000260766.7:c.5157A>T	ENSP00000260766.3:p.Thr1719=
ENST00000371375.1:c.4233A>T	ENSP00000360426.1:p.Thr1411=
ENST00000371380.7:c.5157A>T	ENSP00000360431.2:p.Thr1719=
ENST00000371385.7:c.4233A>T	ENSP00000360438.3:p.Thr1411=
NM_001165979.2:c.4233A>T	NP_001159451.1:p.Thr1411=
NM_001288989.1:c.5109A>T	NP_001275918.1:p.Thr1703=
NM_016341.3:c.5157A>T	NP_057425.3:p.Thr1719=
XM_006717885.2:c.5199A>T	XP_006717948.1:p.Thr1733=
XM_006717886.2:c.5199A>T	XP_006717949.1:p.Thr1733=
XM_006717888.2:c.5196A>T	XP_006717951.1:p.Thr1732=
XM_006717889.2:c.5151A>T	XP_006717952.1:p.Thr1717=
XM_006717890.1:c.4275A>T	XP_006717953.1:p.Thr1425=
XM_011539849.1:c.5199A>T	XP_011538151.1:p.Thr1733=
XM_011539850.1:c.4044A>T	XP_011538152.1:p.Thr1348=
XM_006717885.4:c.5199A>T	XP_006717948.1:p.Thr1733=
XM_006717888.4:c.5196A>T	XP_006717951.1:p.Thr1732=
XM_006717889.4:c.5151A>T	XP_006717952.1:p.Thr1717=
XM_006717890.3:c.4275A>T	XP_006717953.1:p.Thr1425=
XM_011539849.3:c.5199A>T	XP_011538151.1:p.Thr1733=
XM_011539850.3:c.4044A>T	XP_011538152.1:p.Thr1348=
XM_017016310.2:c.5199A>T	XP_016871799.1:p.Thr1733=
XM_017016311.2:c.5199A>T	XP_016871800.1:p.Thr1733=
XM_017016312.2:c.4185A>T	XP_016871801.1:p.Thr1395=
NM_001288989.2:c.5109A>T	NP_001275918.1:p.Thr1703=
NM_016341.4:c.5157A>T MANE Select	NP_057425.3:p.Thr1719=