Canonical Allele Identifier: CA470986402

Gene: PLCE1

Linked Data

• MyVariant Identifiers: chr10:g.96058152T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298395T>C , CM000672.2:g.94298395T>C	GRCh38
NC_000010.10:g.96058152T>C , CM000672.1:g.96058152T>C	GRCh37
NC_000010.9:g.96048142T>C	NCBI36
NG_015799.1:g.309407T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000371375.2:c.4260T>C	ENSP00000360426.1:p.Ile1420=
ENST00000685253.1:c.*1727T>C	ENSP00000509405.1:n.*1727T>C
ENST00000685889.1:n.1919T>C
ENST00000686807.1:n.603T>C
ENST00000686954.1:c.*468T>C	ENSP00000508416.1:n.*468T>C
ENST00000688810.1:c.4212T>C	ENSP00000509140.1:p.Ile1404=
ENST00000689233.1:n.9392T>C
ENST00000690340.1:n.2857T>C
ENST00000692286.1:c.5052T>C	ENSP00000509490.1:p.Ile1684=
ENST00000692396.1:c.5136T>C	ENSP00000508605.1:p.Ile1712=
ENST00000371380.8:c.5184T>C MANE Select	ENSP00000360431.2:p.Ile1728=
ENST00000371385.8:c.4158T>C	ENSP00000360438.4:p.Ile1386=
ENST00000674738.1:c.3739T>C
ENST00000674827.1:c.3300T>C	ENSP00000502523.1:p.Ile1100=
ENST00000675218.1:c.4260T>C	ENSP00000501910.1:p.Ile1420=
ENST00000675487.1:c.*1117T>C	ENSP00000502340.1:n.*1117T>C
ENST00000675718.1:c.4453T>C
ENST00000676102.1:c.4029T>C	ENSP00000502811.1:p.Ile1343=
ENST00000260766.7:c.5184T>C	ENSP00000260766.3:p.Ile1728=
ENST00000371375.1:c.4260T>C	ENSP00000360426.1:p.Ile1420=
ENST00000371380.7:c.5184T>C	ENSP00000360431.2:p.Ile1728=
ENST00000371385.7:c.4260T>C	ENSP00000360438.3:p.Ile1420=
NM_001165979.2:c.4260T>C	NP_001159451.1:p.Ile1420=
NM_001288989.1:c.5136T>C	NP_001275918.1:p.Ile1712=
NM_016341.3:c.5184T>C	NP_057425.3:p.Ile1728=
XM_006717885.2:c.5226T>C	XP_006717948.1:p.Ile1742=
XM_006717886.2:c.5226T>C	XP_006717949.1:p.Ile1742=
XM_006717888.2:c.5223T>C	XP_006717951.1:p.Ile1741=
XM_006717889.2:c.5178T>C	XP_006717952.1:p.Ile1726=
XM_006717890.1:c.4302T>C	XP_006717953.1:p.Ile1434=
XM_011539849.1:c.5226T>C	XP_011538151.1:p.Ile1742=
XM_011539850.1:c.4071T>C	XP_011538152.1:p.Ile1357=
XM_006717885.4:c.5226T>C	XP_006717948.1:p.Ile1742=
XM_006717888.4:c.5223T>C	XP_006717951.1:p.Ile1741=
XM_006717889.4:c.5178T>C	XP_006717952.1:p.Ile1726=
XM_006717890.3:c.4302T>C	XP_006717953.1:p.Ile1434=
XM_011539849.3:c.5226T>C	XP_011538151.1:p.Ile1742=
XM_011539850.3:c.4071T>C	XP_011538152.1:p.Ile1357=
XM_017016310.2:c.5226T>C	XP_016871799.1:p.Ile1742=
XM_017016311.2:c.5226T>C	XP_016871800.1:p.Ile1742=
XM_017016312.2:c.4212T>C	XP_016871801.1:p.Ile1404=
NM_001288989.2:c.5136T>C	NP_001275918.1:p.Ile1712=
NM_016341.4:c.5184T>C MANE Select	NP_057425.3:p.Ile1728=