Canonical Allele Identifier: CA377642399

Gene: PLCE1

Linked Data

• MyVariant Identifiers: chr10:g.96058427G>C (hg19) ; chr10:g.94298670G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298670G>C , CM000672.2:g.94298670G>C	GRCh38
NC_000010.10:g.96058427G>C , CM000672.1:g.96058427G>C	GRCh37
NC_000010.9:g.96048417G>C	NCBI36
NG_015799.1:g.309682G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.4534+1G>C	ENSP00000360426.1:n.4534+1G>C
ENST00000685253.1:c.*2001+1G>C	ENSP00000509405.1:n.*2001+1G>C
ENST00000685889.1:n.2193+1G>C
ENST00000686807.1:n.877+1G>C
ENST00000686954.1:c.*742+1G>C	ENSP00000508416.1:n.*742+1G>C
ENST00000688810.1:c.4486+1G>C	ENSP00000509140.1:n.4486+1G>C
ENST00000689233.1:n.9666+1G>C
ENST00000690340.1:n.3131+1G>C
ENST00000692286.1:c.5326+1G>C	ENSP00000509490.1:n.5326+1G>C
ENST00000692396.1:c.5410+1G>C	ENSP00000508605.1:n.5410+1G>C
ENST00000371380.8:c.5458+1G>C MANE Select	ENSP00000360431.2:n.5458+1G>C
ENST00000371385.8:c.4432+1G>C	ENSP00000360438.4:n.4432+1G>C
ENST00000674738.1:c.4013+1G>C
ENST00000674827.1:c.3574+1G>C	ENSP00000502523.1:n.3574+1G>C
ENST00000675218.1:c.4534+1G>C	ENSP00000501910.1:n.4534+1G>C
ENST00000675487.1:c.*1391+1G>C	ENSP00000502340.1:n.*1391+1G>C
ENST00000675718.1:c.4727+1G>C
ENST00000260766.7:c.5458+1G>C	ENSP00000260766.3:n.5458+1G>C
ENST00000371375.1:c.4534+1G>C	ENSP00000360426.1:n.4534+1G>C
ENST00000371380.7:c.5458+1G>C	ENSP00000360431.2:n.5458+1G>C
ENST00000371385.7:c.4534+1G>C	ENSP00000360438.3:n.4534+1G>C
NM_001165979.2:c.4534+1G>C	NP_001159451.1:n.4534+1G>C
NM_001288989.1:c.5410+1G>C	NP_001275918.1:n.5410+1G>C
NM_016341.3:c.5458+1G>C	NP_057425.3:n.5458+1G>C
XM_006717885.2:c.5500+1G>C	XP_006717948.1:n.5500+1G>C
XM_006717886.2:c.5500+1G>C	XP_006717949.1:n.5500+1G>C
XM_006717888.2:c.5497+1G>C	XP_006717951.1:n.5497+1G>C
XM_006717889.2:c.5452+1G>C	XP_006717952.1:n.5452+1G>C
XM_006717890.1:c.4576+1G>C	XP_006717953.1:n.4576+1G>C
XM_011539849.1:c.5500+1G>C	XP_011538151.1:n.5500+1G>C
XM_011539850.1:c.4345+1G>C	XP_011538152.1:n.4345+1G>C
XM_006717885.4:c.5500+1G>C	XP_006717948.1:n.5500+1G>C
XM_006717888.4:c.5497+1G>C	XP_006717951.1:n.5497+1G>C
XM_006717889.4:c.5452+1G>C	XP_006717952.1:n.5452+1G>C
XM_006717890.3:c.4576+1G>C	XP_006717953.1:n.4576+1G>C
XM_011539849.3:c.5500+1G>C	XP_011538151.1:n.5500+1G>C
XM_011539850.3:c.4345+1G>C	XP_011538152.1:n.4345+1G>C
XM_017016310.2:c.5500+1G>C	XP_016871799.1:n.5500+1G>C
XM_017016311.2:c.5500+1G>C	XP_016871800.1:n.5500+1G>C
XM_017016312.2:c.4486+1G>C	XP_016871801.1:n.4486+1G>C
NM_001288989.2:c.5410+1G>C	NP_001275918.1:n.5410+1G>C
NM_016341.4:c.5458+1G>C MANE Select	NP_057425.3:n.5458+1G>C