Canonical Allele Identifier: CA377641761

Gene: PLCE1

Linked Data

• MyVariant Identifiers: chr10:g.96058189C>A (hg19) ; chr10:g.94298432C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298432C>A , CM000672.2:g.94298432C>A	GRCh38
NC_000010.10:g.96058189C>A , CM000672.1:g.96058189C>A	GRCh37
NC_000010.9:g.96048179C>A	NCBI36
NG_015799.1:g.309444C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.4297C>A	ENSP00000360426.1:p.Pro1433Thr
ENST00000685253.1:c.*1764C>A	ENSP00000509405.1:n.*1764C>A
ENST00000685889.1:n.1956C>A
ENST00000686807.1:n.640C>A
ENST00000686954.1:c.*505C>A	ENSP00000508416.1:n.*505C>A
ENST00000688810.1:c.4249C>A	ENSP00000509140.1:p.Pro1417Thr
ENST00000689233.1:n.9429C>A
ENST00000690340.1:n.2894C>A
ENST00000692286.1:c.5089C>A	ENSP00000509490.1:p.Pro1697Thr
ENST00000692396.1:c.5173C>A	ENSP00000508605.1:p.Pro1725Thr
ENST00000371380.8:c.5221C>A MANE Select	ENSP00000360431.2:p.Pro1741Thr
ENST00000371385.8:c.4195C>A	ENSP00000360438.4:p.Pro1399Thr
ENST00000674738.1:c.3776C>A
ENST00000674827.1:c.3337C>A	ENSP00000502523.1:p.Pro1113Thr
ENST00000675218.1:c.4297C>A	ENSP00000501910.1:p.Pro1433Thr
ENST00000675487.1:c.*1154C>A	ENSP00000502340.1:n.*1154C>A
ENST00000675718.1:c.4490C>A
ENST00000676102.1:c.4066C>A	ENSP00000502811.1:p.Pro1356Thr
ENST00000260766.7:c.5221C>A	ENSP00000260766.3:p.Pro1741Thr
ENST00000371375.1:c.4297C>A	ENSP00000360426.1:p.Pro1433Thr
ENST00000371380.7:c.5221C>A	ENSP00000360431.2:p.Pro1741Thr
ENST00000371385.7:c.4297C>A	ENSP00000360438.3:p.Pro1433Thr
NM_001165979.2:c.4297C>A	NP_001159451.1:p.Pro1433Thr
NM_001288989.1:c.5173C>A	NP_001275918.1:p.Pro1725Thr
NM_016341.3:c.5221C>A	NP_057425.3:p.Pro1741Thr
XM_006717885.2:c.5263C>A	XP_006717948.1:p.Pro1755Thr
XM_006717886.2:c.5263C>A	XP_006717949.1:p.Pro1755Thr
XM_006717888.2:c.5260C>A	XP_006717951.1:p.Pro1754Thr
XM_006717889.2:c.5215C>A	XP_006717952.1:p.Pro1739Thr
XM_006717890.1:c.4339C>A	XP_006717953.1:p.Pro1447Thr
XM_011539849.1:c.5263C>A	XP_011538151.1:p.Pro1755Thr
XM_011539850.1:c.4108C>A	XP_011538152.1:p.Pro1370Thr
XM_006717885.4:c.5263C>A	XP_006717948.1:p.Pro1755Thr
XM_006717888.4:c.5260C>A	XP_006717951.1:p.Pro1754Thr
XM_006717889.4:c.5215C>A	XP_006717952.1:p.Pro1739Thr
XM_006717890.3:c.4339C>A	XP_006717953.1:p.Pro1447Thr
XM_011539849.3:c.5263C>A	XP_011538151.1:p.Pro1755Thr
XM_011539850.3:c.4108C>A	XP_011538152.1:p.Pro1370Thr
XM_017016310.2:c.5263C>A	XP_016871799.1:p.Pro1755Thr
XM_017016311.2:c.5263C>A	XP_016871800.1:p.Pro1755Thr
XM_017016312.2:c.4249C>A	XP_016871801.1:p.Pro1417Thr
NM_001288989.2:c.5173C>A	NP_001275918.1:p.Pro1725Thr
NM_016341.4:c.5221C>A MANE Select	NP_057425.3:p.Pro1741Thr