Canonical Allele Identifier: CA377651740

Gene: PLCE1 PLCE1-AS1

Linked Data

• MyVariant Identifiers: chr10:g.96039602G>T (hg19) ; chr10:g.94279845G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94279845G>T , CM000672.2:g.94279845G>T	GRCh38
NC_000010.10:g.96039602G>T , CM000672.1:g.96039602G>T	GRCh37
NC_000010.9:g.96029592G>T	NCBI36
NG_015799.1:g.290857G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371375.2:c.3805G>T (PLCE1)	ENSP00000360426.1:p.Ala1269Ser
ENST00000685253.1:c.*1272G>T (PLCE1)	ENSP00000509405.1:n.*1272G>T
ENST00000685889.1:n.1464G>T (PLCE1)
ENST00000686954.1:c.4729G>T (PLCE1)	ENSP00000508416.1:p.Ala1577Ser
ENST00000688810.1:c.3757G>T (PLCE1)	ENSP00000509140.1:p.Ala1253Ser
ENST00000689233.1:n.5059G>T (PLCE1)
ENST00000692286.1:c.4729G>T (PLCE1)	ENSP00000509490.1:p.Ala1577Ser
ENST00000692396.1:c.4681G>T (PLCE1)	ENSP00000508605.1:p.Ala1561Ser
ENST00000371380.8:c.4729G>T (PLCE1) MANE Select	ENSP00000360431.2:p.Ala1577Ser
ENST00000371385.8:c.3703G>T (PLCE1)	ENSP00000360438.4:p.Ala1235Ser
ENST00000674738.1:c.3134G>T (PLCE1)
ENST00000674827.1:c.2806G>T (PLCE1)	ENSP00000502523.1:p.Ala936Ser
ENST00000675218.1:c.3805G>T (PLCE1)	ENSP00000501910.1:p.Ala1269Ser
ENST00000675487.1:c.*662G>T (PLCE1)	ENSP00000502340.1:n.*662G>T
ENST00000675718.1:c.3956G>T (PLCE1)
ENST00000676102.1:c.3574G>T (PLCE1)	ENSP00000502811.1:p.Ala1192Ser
ENST00000260766.7:c.4729G>T (PLCE1)	ENSP00000260766.3:p.Ala1577Ser
ENST00000371375.1:c.3805G>T (PLCE1)	ENSP00000360426.1:p.Ala1269Ser
ENST00000371380.7:c.4729G>T (PLCE1)	ENSP00000360431.2:p.Ala1577Ser
ENST00000371385.7:c.3805G>T (PLCE1)	ENSP00000360438.3:p.Ala1269Ser
NM_001165979.2:c.3805G>T (PLCE1)	NP_001159451.1:p.Ala1269Ser
NM_001288989.1:c.4681G>T (PLCE1)	NP_001275918.1:p.Ala1561Ser
NM_016341.3:c.4729G>T (PLCE1)	NP_057425.3:p.Ala1577Ser
NR_033969.1:n.853C>A (PLCE1-AS1)
XM_006717885.2:c.4729G>T (PLCE1)	XP_006717948.1:p.Ala1577Ser
XM_006717886.2:c.4729G>T (PLCE1)	XP_006717949.1:p.Ala1577Ser
XM_006717888.2:c.4729G>T (PLCE1)	XP_006717951.1:p.Ala1577Ser
XM_006717889.2:c.4681G>T (PLCE1)	XP_006717952.1:p.Ala1561Ser
XM_006717890.1:c.3805G>T (PLCE1)	XP_006717953.1:p.Ala1269Ser
XM_011539849.1:c.4729G>T (PLCE1)	XP_011538151.1:p.Ala1577Ser
XM_011539850.1:c.3574G>T (PLCE1)	XP_011538152.1:p.Ala1192Ser
XM_011539851.1:c.4729G>T (PLCE1)	XP_011538153.1:p.Ala1577Ser
XM_011539852.1:c.4729G>T (PLCE1)	XP_011538154.1:p.Ala1577Ser
XM_006717885.4:c.4729G>T (PLCE1)	XP_006717948.1:p.Ala1577Ser
XM_006717888.4:c.4729G>T (PLCE1)	XP_006717951.1:p.Ala1577Ser
XM_006717889.4:c.4681G>T (PLCE1)	XP_006717952.1:p.Ala1561Ser
XM_006717890.3:c.3805G>T (PLCE1)	XP_006717953.1:p.Ala1269Ser
XM_011539849.3:c.4729G>T (PLCE1)	XP_011538151.1:p.Ala1577Ser
XM_011539850.3:c.3574G>T (PLCE1)	XP_011538152.1:p.Ala1192Ser
XM_011539851.3:c.4729G>T (PLCE1)	XP_011538153.1:p.Ala1577Ser
XM_011539852.3:c.4729G>T (PLCE1)	XP_011538154.1:p.Ala1577Ser
XM_017016310.2:c.4729G>T (PLCE1)	XP_016871799.1:p.Ala1577Ser
XM_017016311.2:c.4729G>T (PLCE1)	XP_016871800.1:p.Ala1577Ser
XM_017016312.2:c.3757G>T (PLCE1)	XP_016871801.1:p.Ala1253Ser
NM_001288989.2:c.4681G>T (PLCE1)	NP_001275918.1:p.Ala1561Ser
NM_016341.4:c.4729G>T (PLCE1) MANE Select	NP_057425.3:p.Ala1577Ser