Canonical Allele Identifier: CA5613328

Gene: PLCE1

Linked Data

• dbSNP Id: rs544095097
• ExAC: 10:96058258 G / T
• gnomAD v2: 10-96058258-G-T
• gnomAD v3: 10-94298501-G-T
• gnomAD v4: 10-94298501-G-T
• COSMIC: COSM4188767 ; COSM4188768 ; COSM4188769
• MyVariant Identifiers: chr10:g.96058258G>T (hg19) ; chr10:g.94298501G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298501G>T , CM000672.2:g.94298501G>T	GRCh38
NC_000010.10:g.96058258G>T , CM000672.1:g.96058258G>T	GRCh37
NC_000010.9:g.96048248G>T	NCBI36
NG_015799.1:g.309513G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371375.2:c.4366G>T	ENSP00000360426.1:p.Ala1456Ser
ENST00000685253.1:c.*1833G>T	ENSP00000509405.1:n.*1833G>T
ENST00000685889.1:n.2025G>T
ENST00000686807.1:n.709G>T
ENST00000686954.1:c.*574G>T	ENSP00000508416.1:n.*574G>T
ENST00000688810.1:c.4318G>T	ENSP00000509140.1:p.Ala1440Ser
ENST00000689233.1:n.9498G>T
ENST00000690340.1:n.2963G>T
ENST00000692286.1:c.5158G>T	ENSP00000509490.1:p.Ala1720Ser
ENST00000692396.1:c.5242G>T	ENSP00000508605.1:p.Ala1748Ser
ENST00000371380.8:c.5290G>T MANE Select	ENSP00000360431.2:p.Ala1764Ser
ENST00000371385.8:c.4264G>T	ENSP00000360438.4:p.Ala1422Ser
ENST00000674738.1:c.3845G>T
ENST00000674827.1:c.3406G>T	ENSP00000502523.1:p.Ala1136Ser
ENST00000675218.1:c.4366G>T	ENSP00000501910.1:p.Ala1456Ser
ENST00000675487.1:c.*1223G>T	ENSP00000502340.1:n.*1223G>T
ENST00000675718.1:c.4559G>T
ENST00000260766.7:c.5290G>T	ENSP00000260766.3:p.Ala1764Ser
ENST00000371375.1:c.4366G>T	ENSP00000360426.1:p.Ala1456Ser
ENST00000371380.7:c.5290G>T	ENSP00000360431.2:p.Ala1764Ser
ENST00000371385.7:c.4366G>T	ENSP00000360438.3:p.Ala1456Ser
NM_001165979.2:c.4366G>T	NP_001159451.1:p.Ala1456Ser
NM_001288989.1:c.5242G>T	NP_001275918.1:p.Ala1748Ser
NM_016341.3:c.5290G>T	NP_057425.3:p.Ala1764Ser
XM_006717885.2:c.5332G>T	XP_006717948.1:p.Ala1778Ser
XM_006717886.2:c.5332G>T	XP_006717949.1:p.Ala1778Ser
XM_006717888.2:c.5329G>T	XP_006717951.1:p.Ala1777Ser
XM_006717889.2:c.5284G>T	XP_006717952.1:p.Ala1762Ser
XM_006717890.1:c.4408G>T	XP_006717953.1:p.Ala1470Ser
XM_011539849.1:c.5332G>T	XP_011538151.1:p.Ala1778Ser
XM_011539850.1:c.4177G>T	XP_011538152.1:p.Ala1393Ser
XM_006717885.4:c.5332G>T	XP_006717948.1:p.Ala1778Ser
XM_006717888.4:c.5329G>T	XP_006717951.1:p.Ala1777Ser
XM_006717889.4:c.5284G>T	XP_006717952.1:p.Ala1762Ser
XM_006717890.3:c.4408G>T	XP_006717953.1:p.Ala1470Ser
XM_011539849.3:c.5332G>T	XP_011538151.1:p.Ala1778Ser
XM_011539850.3:c.4177G>T	XP_011538152.1:p.Ala1393Ser
XM_017016310.2:c.5332G>T	XP_016871799.1:p.Ala1778Ser
XM_017016311.2:c.5332G>T	XP_016871800.1:p.Ala1778Ser
XM_017016312.2:c.4318G>T	XP_016871801.1:p.Ala1440Ser
NM_001288989.2:c.5242G>T	NP_001275918.1:p.Ala1748Ser
NM_016341.4:c.5290G>T MANE Select	NP_057425.3:p.Ala1764Ser