Canonical Allele Identifier: CA377641935

Gene: PLCE1

Linked Data

• MyVariant Identifiers: chr10:g.96058268G>C (hg19) ; chr10:g.94298511G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298511G>C , CM000672.2:g.94298511G>C	GRCh38
NC_000010.10:g.96058268G>C , CM000672.1:g.96058268G>C	GRCh37
NC_000010.9:g.96048258G>C	NCBI36
NG_015799.1:g.309523G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.4376G>C	ENSP00000360426.1:p.Arg1459Pro
ENST00000685253.1:c.*1843G>C	ENSP00000509405.1:n.*1843G>C
ENST00000685889.1:n.2035G>C
ENST00000686807.1:n.719G>C
ENST00000686954.1:c.*584G>C	ENSP00000508416.1:n.*584G>C
ENST00000688810.1:c.4328G>C	ENSP00000509140.1:p.Arg1443Pro
ENST00000689233.1:n.9508G>C
ENST00000690340.1:n.2973G>C
ENST00000692286.1:c.5168G>C	ENSP00000509490.1:p.Arg1723Pro
ENST00000692396.1:c.5252G>C	ENSP00000508605.1:p.Arg1751Pro
ENST00000371380.8:c.5300G>C MANE Select	ENSP00000360431.2:p.Arg1767Pro
ENST00000371385.8:c.4274G>C	ENSP00000360438.4:p.Arg1425Pro
ENST00000674738.1:c.3855G>C
ENST00000674827.1:c.3416G>C	ENSP00000502523.1:p.Arg1139Pro
ENST00000675218.1:c.4376G>C	ENSP00000501910.1:p.Arg1459Pro
ENST00000675487.1:c.*1233G>C	ENSP00000502340.1:n.*1233G>C
ENST00000675718.1:c.4569G>C
ENST00000260766.7:c.5300G>C	ENSP00000260766.3:p.Arg1767Pro
ENST00000371375.1:c.4376G>C	ENSP00000360426.1:p.Arg1459Pro
ENST00000371380.7:c.5300G>C	ENSP00000360431.2:p.Arg1767Pro
ENST00000371385.7:c.4376G>C	ENSP00000360438.3:p.Arg1459Pro
NM_001165979.2:c.4376G>C	NP_001159451.1:p.Arg1459Pro
NM_001288989.1:c.5252G>C	NP_001275918.1:p.Arg1751Pro
NM_016341.3:c.5300G>C	NP_057425.3:p.Arg1767Pro
XM_006717885.2:c.5342G>C	XP_006717948.1:p.Arg1781Pro
XM_006717886.2:c.5342G>C	XP_006717949.1:p.Arg1781Pro
XM_006717888.2:c.5339G>C	XP_006717951.1:p.Arg1780Pro
XM_006717889.2:c.5294G>C	XP_006717952.1:p.Arg1765Pro
XM_006717890.1:c.4418G>C	XP_006717953.1:p.Arg1473Pro
XM_011539849.1:c.5342G>C	XP_011538151.1:p.Arg1781Pro
XM_011539850.1:c.4187G>C	XP_011538152.1:p.Arg1396Pro
XM_006717885.4:c.5342G>C	XP_006717948.1:p.Arg1781Pro
XM_006717888.4:c.5339G>C	XP_006717951.1:p.Arg1780Pro
XM_006717889.4:c.5294G>C	XP_006717952.1:p.Arg1765Pro
XM_006717890.3:c.4418G>C	XP_006717953.1:p.Arg1473Pro
XM_011539849.3:c.5342G>C	XP_011538151.1:p.Arg1781Pro
XM_011539850.3:c.4187G>C	XP_011538152.1:p.Arg1396Pro
XM_017016310.2:c.5342G>C	XP_016871799.1:p.Arg1781Pro
XM_017016311.2:c.5342G>C	XP_016871800.1:p.Arg1781Pro
XM_017016312.2:c.4328G>C	XP_016871801.1:p.Arg1443Pro
NM_001288989.2:c.5252G>C	NP_001275918.1:p.Arg1751Pro
NM_016341.4:c.5300G>C MANE Select	NP_057425.3:p.Arg1767Pro