Canonical Allele Identifier: CA470986611

Gene: PLCE1

Linked Data

• MyVariant Identifiers: chr10:g.96058356T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298599T>C , CM000672.2:g.94298599T>C	GRCh38
NC_000010.10:g.96058356T>C , CM000672.1:g.96058356T>C	GRCh37
NC_000010.9:g.96048346T>C	NCBI36
NG_015799.1:g.309611T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000371375.2:c.4464T>C	ENSP00000360426.1:p.Ser1488=
ENST00000685253.1:c.*1931T>C	ENSP00000509405.1:n.*1931T>C
ENST00000685889.1:n.2123T>C
ENST00000686807.1:n.807T>C
ENST00000686954.1:c.*672T>C	ENSP00000508416.1:n.*672T>C
ENST00000688810.1:c.4416T>C	ENSP00000509140.1:p.Ser1472=
ENST00000689233.1:n.9596T>C
ENST00000690340.1:n.3061T>C
ENST00000692286.1:c.5256T>C	ENSP00000509490.1:p.Ser1752=
ENST00000692396.1:c.5340T>C	ENSP00000508605.1:p.Ser1780=
ENST00000371380.8:c.5388T>C MANE Select	ENSP00000360431.2:p.Ser1796=
ENST00000371385.8:c.4362T>C	ENSP00000360438.4:p.Ser1454=
ENST00000674738.1:c.3943T>C
ENST00000674827.1:c.3504T>C	ENSP00000502523.1:p.Ser1168=
ENST00000675218.1:c.4464T>C	ENSP00000501910.1:p.Ser1488=
ENST00000675487.1:c.*1321T>C	ENSP00000502340.1:n.*1321T>C
ENST00000675718.1:c.4657T>C
ENST00000260766.7:c.5388T>C	ENSP00000260766.3:p.Ser1796=
ENST00000371375.1:c.4464T>C	ENSP00000360426.1:p.Ser1488=
ENST00000371380.7:c.5388T>C	ENSP00000360431.2:p.Ser1796=
ENST00000371385.7:c.4464T>C	ENSP00000360438.3:p.Ser1488=
NM_001165979.2:c.4464T>C	NP_001159451.1:p.Ser1488=
NM_001288989.1:c.5340T>C	NP_001275918.1:p.Ser1780=
NM_016341.3:c.5388T>C	NP_057425.3:p.Ser1796=
XM_006717885.2:c.5430T>C	XP_006717948.1:p.Ser1810=
XM_006717886.2:c.5430T>C	XP_006717949.1:p.Ser1810=
XM_006717888.2:c.5427T>C	XP_006717951.1:p.Ser1809=
XM_006717889.2:c.5382T>C	XP_006717952.1:p.Ser1794=
XM_006717890.1:c.4506T>C	XP_006717953.1:p.Ser1502=
XM_011539849.1:c.5430T>C	XP_011538151.1:p.Ser1810=
XM_011539850.1:c.4275T>C	XP_011538152.1:p.Ser1425=
XM_006717885.4:c.5430T>C	XP_006717948.1:p.Ser1810=
XM_006717888.4:c.5427T>C	XP_006717951.1:p.Ser1809=
XM_006717889.4:c.5382T>C	XP_006717952.1:p.Ser1794=
XM_006717890.3:c.4506T>C	XP_006717953.1:p.Ser1502=
XM_011539849.3:c.5430T>C	XP_011538151.1:p.Ser1810=
XM_011539850.3:c.4275T>C	XP_011538152.1:p.Ser1425=
XM_017016310.2:c.5430T>C	XP_016871799.1:p.Ser1810=
XM_017016311.2:c.5430T>C	XP_016871800.1:p.Ser1810=
XM_017016312.2:c.4416T>C	XP_016871801.1:p.Ser1472=
NM_001288989.2:c.5340T>C	NP_001275918.1:p.Ser1780=
NM_016341.4:c.5388T>C MANE Select	NP_057425.3:p.Ser1796=