Canonical Allele Identifier: CA2610239406

Gene: PLCE1

Linked Data

• gnomAD v4: 10-94293479-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94293479G>C , CM000672.2:g.94293479G>C	GRCh38
NC_000010.10:g.96053236G>C , CM000672.1:g.96053236G>C	GRCh37
NC_000010.9:g.96043226G>C	NCBI36
NG_015799.1:g.304491G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.4112-29G>C	ENSP00000360426.1:n.4112-29G>C
ENST00000685253.1:c.*1579-29G>C	ENSP00000509405.1:n.*1579-29G>C
ENST00000685889.1:n.1771-29G>C
ENST00000686807.1:n.426G>C
ENST00000686954.1:c.*320-29G>C	ENSP00000508416.1:n.*320-29G>C
ENST00000688810.1:c.4064-29G>C	ENSP00000509140.1:n.4064-29G>C
ENST00000689233.1:n.9244-29G>C
ENST00000690340.1:n.2709-29G>C
ENST00000692286.1:c.5036-4900G>C	ENSP00000509490.1:n.5036-4900G>C
ENST00000692396.1:c.4988-29G>C	ENSP00000508605.1:n.4988-29G>C
ENST00000371380.8:c.5036-29G>C MANE Select	ENSP00000360431.2:n.5036-29G>C
ENST00000371385.8:c.4010-29G>C	ENSP00000360438.4:n.4010-29G>C
ENST00000674738.1:c.3591-29G>C
ENST00000674827.1:c.3152-29G>C	ENSP00000502523.1:n.3152-29G>C
ENST00000675218.1:c.4112-29G>C	ENSP00000501910.1:n.4112-29G>C
ENST00000675487.1:c.*969-29G>C	ENSP00000502340.1:n.*969-29G>C
ENST00000675718.1:c.4305-29G>C
ENST00000676102.1:c.3881-29G>C	ENSP00000502811.1:n.3881-29G>C
ENST00000260766.7:c.5036-29G>C	ENSP00000260766.3:n.5036-29G>C
ENST00000371375.1:c.4112-29G>C	ENSP00000360426.1:n.4112-29G>C
ENST00000371380.7:c.5036-29G>C	ENSP00000360431.2:n.5036-29G>C
ENST00000371385.7:c.4112-29G>C	ENSP00000360438.3:n.4112-29G>C
NM_001165979.2:c.4112-29G>C	NP_001159451.1:n.4112-29G>C
NM_001288989.1:c.4988-29G>C	NP_001275918.1:n.4988-29G>C
NM_016341.3:c.5036-29G>C	NP_057425.3:n.5036-29G>C
XM_006717885.2:c.5078-29G>C	XP_006717948.1:n.5078-29G>C
XM_006717886.2:c.5078-29G>C	XP_006717949.1:n.5078-29G>C
XM_006717888.2:c.5075-29G>C	XP_006717951.1:n.5075-29G>C
XM_006717889.2:c.5030-29G>C	XP_006717952.1:n.5030-29G>C
XM_006717890.1:c.4154-29G>C	XP_006717953.1:n.4154-29G>C
XM_011539849.1:c.5078-29G>C	XP_011538151.1:n.5078-29G>C
XM_011539850.1:c.3923-29G>C	XP_011538152.1:n.3923-29G>C
XM_006717885.4:c.5078-29G>C	XP_006717948.1:n.5078-29G>C
XM_006717888.4:c.5075-29G>C	XP_006717951.1:n.5075-29G>C
XM_006717889.4:c.5030-29G>C	XP_006717952.1:n.5030-29G>C
XM_006717890.3:c.4154-29G>C	XP_006717953.1:n.4154-29G>C
XM_011539849.3:c.5078-29G>C	XP_011538151.1:n.5078-29G>C
XM_011539850.3:c.3923-29G>C	XP_011538152.1:n.3923-29G>C
XM_017016310.2:c.5078-29G>C	XP_016871799.1:n.5078-29G>C
XM_017016311.2:c.5078-29G>C	XP_016871800.1:n.5078-29G>C
XM_017016312.2:c.4064-29G>C	XP_016871801.1:n.4064-29G>C
NM_001288989.2:c.4988-29G>C	NP_001275918.1:n.4988-29G>C
NM_016341.4:c.5036-29G>C MANE Select	NP_057425.3:n.5036-29G>C