Canonical Allele Identifier: CA5613134

Gene: PLCE1

Linked Data

• dbSNP Id: rs752465893
• ExAC: 10:96030259 T / C
• gnomAD v2: 10-96030259-T-C
• gnomAD v4: 10-94270502-T-C
• MyVariant Identifiers: chr10:g.96030259T>C (hg19) ; chr10:g.94270502T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94270502T>C , CM000672.2:g.94270502T>C	GRCh38
NC_000010.10:g.96030259T>C , CM000672.1:g.96030259T>C	GRCh37
NC_000010.9:g.96020249T>C	NCBI36
NG_015799.1:g.281514T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.3482T>C	ENSP00000360426.1:p.Ile1161Thr
ENST00000685253.1:c.*949T>C	ENSP00000509405.1:n.*949T>C
ENST00000685889.1:n.1141T>C
ENST00000686954.1:c.4406T>C	ENSP00000508416.1:p.Ile1469Thr
ENST00000688810.1:c.3434T>C	ENSP00000509140.1:p.Ile1145Thr
ENST00000689233.1:n.4736T>C
ENST00000692286.1:c.4406T>C	ENSP00000509490.1:p.Ile1469Thr
ENST00000692396.1:c.4358T>C	ENSP00000508605.1:p.Ile1453Thr
ENST00000371380.8:c.4406T>C MANE Select	ENSP00000360431.2:p.Ile1469Thr
ENST00000371385.8:c.3380T>C	ENSP00000360438.4:p.Ile1127Thr
ENST00000674738.1:c.2811T>C
ENST00000674827.1:c.2483T>C	ENSP00000502523.1:p.Ile828Thr
ENST00000675218.1:c.3482T>C	ENSP00000501910.1:p.Ile1161Thr
ENST00000675487.1:c.*339T>C	ENSP00000502340.1:n.*339T>C
ENST00000675718.1:c.3633T>C
ENST00000676102.1:c.3251T>C	ENSP00000502811.1:p.Ile1084Thr
ENST00000260766.7:c.4406T>C	ENSP00000260766.3:p.Ile1469Thr
ENST00000371375.1:c.3482T>C	ENSP00000360426.1:p.Ile1161Thr
ENST00000371380.7:c.4406T>C	ENSP00000360431.2:p.Ile1469Thr
ENST00000371385.7:c.3482T>C	ENSP00000360438.3:p.Ile1161Thr
NM_001165979.2:c.3482T>C	NP_001159451.1:p.Ile1161Thr
NM_001288989.1:c.4358T>C	NP_001275918.1:p.Ile1453Thr
NM_016341.3:c.4406T>C	NP_057425.3:p.Ile1469Thr
XM_006717885.2:c.4406T>C	XP_006717948.1:p.Ile1469Thr
XM_006717886.2:c.4406T>C	XP_006717949.1:p.Ile1469Thr
XM_006717888.2:c.4406T>C	XP_006717951.1:p.Ile1469Thr
XM_006717889.2:c.4358T>C	XP_006717952.1:p.Ile1453Thr
XM_006717890.1:c.3482T>C	XP_006717953.1:p.Ile1161Thr
XM_011539849.1:c.4406T>C	XP_011538151.1:p.Ile1469Thr
XM_011539850.1:c.3251T>C	XP_011538152.1:p.Ile1084Thr
XM_011539851.1:c.4406T>C	XP_011538153.1:p.Ile1469Thr
XM_011539852.1:c.4406T>C	XP_011538154.1:p.Ile1469Thr
XM_006717885.4:c.4406T>C	XP_006717948.1:p.Ile1469Thr
XM_006717888.4:c.4406T>C	XP_006717951.1:p.Ile1469Thr
XM_006717889.4:c.4358T>C	XP_006717952.1:p.Ile1453Thr
XM_006717890.3:c.3482T>C	XP_006717953.1:p.Ile1161Thr
XM_011539849.3:c.4406T>C	XP_011538151.1:p.Ile1469Thr
XM_011539850.3:c.3251T>C	XP_011538152.1:p.Ile1084Thr
XM_011539851.3:c.4406T>C	XP_011538153.1:p.Ile1469Thr
XM_011539852.3:c.4406T>C	XP_011538154.1:p.Ile1469Thr
XM_017016310.2:c.4406T>C	XP_016871799.1:p.Ile1469Thr
XM_017016311.2:c.4406T>C	XP_016871800.1:p.Ile1469Thr
XM_017016312.2:c.3434T>C	XP_016871801.1:p.Ile1145Thr
NM_001288989.2:c.4358T>C	NP_001275918.1:p.Ile1453Thr
NM_016341.4:c.4406T>C MANE Select	NP_057425.3:p.Ile1469Thr