Canonical Allele Identifier: CA470986583

Gene: PLCE1

Linked Data

• dbSNP Id: rs2052924609
• MyVariant Identifiers: chr10:g.96058329T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298572T>C , CM000672.2:g.94298572T>C	GRCh38
NC_000010.10:g.96058329T>C , CM000672.1:g.96058329T>C	GRCh37
NC_000010.9:g.96048319T>C	NCBI36
NG_015799.1:g.309584T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000371375.2:c.4437T>C	ENSP00000360426.1:p.Thr1479=
ENST00000685253.1:c.*1904T>C	ENSP00000509405.1:n.*1904T>C
ENST00000685889.1:n.2096T>C
ENST00000686807.1:n.780T>C
ENST00000686954.1:c.*645T>C	ENSP00000508416.1:n.*645T>C
ENST00000688810.1:c.4389T>C	ENSP00000509140.1:p.Thr1463=
ENST00000689233.1:n.9569T>C
ENST00000690340.1:n.3034T>C
ENST00000692286.1:c.5229T>C	ENSP00000509490.1:p.Thr1743=
ENST00000692396.1:c.5313T>C	ENSP00000508605.1:p.Thr1771=
ENST00000371380.8:c.5361T>C MANE Select	ENSP00000360431.2:p.Thr1787=
ENST00000371385.8:c.4335T>C	ENSP00000360438.4:p.Thr1445=
ENST00000674738.1:c.3916T>C
ENST00000674827.1:c.3477T>C	ENSP00000502523.1:p.Thr1159=
ENST00000675218.1:c.4437T>C	ENSP00000501910.1:p.Thr1479=
ENST00000675487.1:c.*1294T>C	ENSP00000502340.1:n.*1294T>C
ENST00000675718.1:c.4630T>C
ENST00000260766.7:c.5361T>C	ENSP00000260766.3:p.Thr1787=
ENST00000371375.1:c.4437T>C	ENSP00000360426.1:p.Thr1479=
ENST00000371380.7:c.5361T>C	ENSP00000360431.2:p.Thr1787=
ENST00000371385.7:c.4437T>C	ENSP00000360438.3:p.Thr1479=
NM_001165979.2:c.4437T>C	NP_001159451.1:p.Thr1479=
NM_001288989.1:c.5313T>C	NP_001275918.1:p.Thr1771=
NM_016341.3:c.5361T>C	NP_057425.3:p.Thr1787=
XM_006717885.2:c.5403T>C	XP_006717948.1:p.Thr1801=
XM_006717886.2:c.5403T>C	XP_006717949.1:p.Thr1801=
XM_006717888.2:c.5400T>C	XP_006717951.1:p.Thr1800=
XM_006717889.2:c.5355T>C	XP_006717952.1:p.Thr1785=
XM_006717890.1:c.4479T>C	XP_006717953.1:p.Thr1493=
XM_011539849.1:c.5403T>C	XP_011538151.1:p.Thr1801=
XM_011539850.1:c.4248T>C	XP_011538152.1:p.Thr1416=
XM_006717885.4:c.5403T>C	XP_006717948.1:p.Thr1801=
XM_006717888.4:c.5400T>C	XP_006717951.1:p.Thr1800=
XM_006717889.4:c.5355T>C	XP_006717952.1:p.Thr1785=
XM_006717890.3:c.4479T>C	XP_006717953.1:p.Thr1493=
XM_011539849.3:c.5403T>C	XP_011538151.1:p.Thr1801=
XM_011539850.3:c.4248T>C	XP_011538152.1:p.Thr1416=
XM_017016310.2:c.5403T>C	XP_016871799.1:p.Thr1801=
XM_017016311.2:c.5403T>C	XP_016871800.1:p.Thr1801=
XM_017016312.2:c.4389T>C	XP_016871801.1:p.Thr1463=
NM_001288989.2:c.5313T>C	NP_001275918.1:p.Thr1771=
NM_016341.4:c.5361T>C MANE Select	NP_057425.3:p.Thr1787=