Canonical Allele Identifier: CA470986421

Gene: PLCE1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298419T>C , CM000672.2:g.94298419T>C	GRCh38
NC_000010.10:g.96058176T>C , CM000672.1:g.96058176T>C	GRCh37
NC_000010.9:g.96048166T>C	NCBI36
NG_015799.1:g.309431T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_016341.4:c.5208T>C MANE Select	NP_057425.3:p.Ser1736=
ENST00000371380.8:c.5208T>C MANE Select	ENSP00000360431.2:p.Ser1736=
NM_001165979.2:c.4284T>C	NP_001159451.1:p.Ser1428=
NM_001288989.1:c.5160T>C	NP_001275918.1:p.Ser1720=
NM_001288989.2:c.5160T>C	NP_001275918.1:p.Ser1720=
NM_016341.3:c.5208T>C	NP_057425.3:p.Ser1736=
ENST00000260766.7:c.5208T>C	ENSP00000260766.3:p.Ser1736=
ENST00000371375.1:c.4284T>C	ENSP00000360426.1:p.Ser1428=
ENST00000371375.2:c.4284T>C	ENSP00000360426.1:p.Ser1428=
ENST00000371380.7:c.5208T>C	ENSP00000360431.2:p.Ser1736=
ENST00000371385.7:c.4284T>C	ENSP00000360438.3:p.Ser1428=
ENST00000371385.8:c.4182T>C	ENSP00000360438.4:p.Ser1394=
ENST00000674738.1:c.3763T>C
ENST00000674827.1:c.3324T>C	ENSP00000502523.1:p.Ser1108=
ENST00000675218.1:c.4284T>C	ENSP00000501910.1:p.Ser1428=
ENST00000675487.1:c.*1141T>C	ENSP00000502340.1:n.*1141T>C
ENST00000675718.1:c.4477T>C
ENST00000676102.1:c.4053T>C	ENSP00000502811.1:p.Ser1351=
ENST00000685253.1:c.*1751T>C	ENSP00000509405.1:n.*1751T>C
ENST00000685889.1:n.1943T>C
ENST00000686807.1:n.627T>C
ENST00000686954.1:c.*492T>C	ENSP00000508416.1:n.*492T>C
ENST00000688810.1:c.4236T>C	ENSP00000509140.1:p.Ser1412=
ENST00000689233.1:n.9416T>C
ENST00000690340.1:n.2881T>C
ENST00000692286.1:c.5076T>C	ENSP00000509490.1:p.Ser1692=
ENST00000692396.1:c.5160T>C	ENSP00000508605.1:p.Ser1720=
XM_006717885.2:c.5250T>C	XP_006717948.1:p.Ser1750=
XM_006717885.4:c.5250T>C	XP_006717948.1:p.Ser1750=
XM_006717886.2:c.5250T>C	XP_006717949.1:p.Ser1750=
XM_006717888.2:c.5247T>C	XP_006717951.1:p.Ser1749=
XM_006717888.4:c.5247T>C	XP_006717951.1:p.Ser1749=
XM_006717889.2:c.5202T>C	XP_006717952.1:p.Ser1734=
XM_006717889.4:c.5202T>C	XP_006717952.1:p.Ser1734=
XM_006717890.1:c.4326T>C	XP_006717953.1:p.Ser1442=
XM_006717890.3:c.4326T>C	XP_006717953.1:p.Ser1442=
XM_011539849.1:c.5250T>C	XP_011538151.1:p.Ser1750=
XM_011539849.3:c.5250T>C	XP_011538151.1:p.Ser1750=
XM_011539850.1:c.4095T>C	XP_011538152.1:p.Ser1365=
XM_011539850.3:c.4095T>C	XP_011538152.1:p.Ser1365=
XM_017016310.2:c.5250T>C	XP_016871799.1:p.Ser1750=
XM_017016311.2:c.5250T>C	XP_016871800.1:p.Ser1750=
XM_017016312.2:c.4236T>C	XP_016871801.1:p.Ser1412=