Canonical Allele Identifier: CA377651716

Gene: PLCE1 PLCE1-AS1

Linked Data

• MyVariant Identifiers: chr10:g.96039599C>G (hg19) ; chr10:g.94279842C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94279842C>G , CM000672.2:g.94279842C>G	GRCh38
NC_000010.10:g.96039599C>G , CM000672.1:g.96039599C>G	GRCh37
NC_000010.9:g.96029589C>G	NCBI36
NG_015799.1:g.290854C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000371375.2:c.3802C>G (PLCE1)	ENSP00000360426.1:p.Pro1268Ala
ENST00000685253.1:c.*1269C>G (PLCE1)	ENSP00000509405.1:n.*1269C>G
ENST00000685889.1:n.1461C>G (PLCE1)
ENST00000686954.1:c.4726C>G (PLCE1)	ENSP00000508416.1:p.Pro1576Ala
ENST00000688810.1:c.3754C>G (PLCE1)	ENSP00000509140.1:p.Pro1252Ala
ENST00000689233.1:n.5056C>G (PLCE1)
ENST00000692286.1:c.4726C>G (PLCE1)	ENSP00000509490.1:p.Pro1576Ala
ENST00000692396.1:c.4678C>G (PLCE1)	ENSP00000508605.1:p.Pro1560Ala
ENST00000371380.8:c.4726C>G (PLCE1) MANE Select	ENSP00000360431.2:p.Pro1576Ala
ENST00000371385.8:c.3700C>G (PLCE1)	ENSP00000360438.4:p.Pro1234Ala
ENST00000674738.1:c.3131C>G (PLCE1)
ENST00000674827.1:c.2803C>G (PLCE1)	ENSP00000502523.1:p.Pro935Ala
ENST00000675218.1:c.3802C>G (PLCE1)	ENSP00000501910.1:p.Pro1268Ala
ENST00000675487.1:c.*659C>G (PLCE1)	ENSP00000502340.1:n.*659C>G
ENST00000675718.1:c.3953C>G (PLCE1)
ENST00000676102.1:c.3571C>G (PLCE1)	ENSP00000502811.1:p.Pro1191Ala
ENST00000260766.7:c.4726C>G (PLCE1)	ENSP00000260766.3:p.Pro1576Ala
ENST00000371375.1:c.3802C>G (PLCE1)	ENSP00000360426.1:p.Pro1268Ala
ENST00000371380.7:c.4726C>G (PLCE1)	ENSP00000360431.2:p.Pro1576Ala
ENST00000371385.7:c.3802C>G (PLCE1)	ENSP00000360438.3:p.Pro1268Ala
NM_001165979.2:c.3802C>G (PLCE1)	NP_001159451.1:p.Pro1268Ala
NM_001288989.1:c.4678C>G (PLCE1)	NP_001275918.1:p.Pro1560Ala
NM_016341.3:c.4726C>G (PLCE1)	NP_057425.3:p.Pro1576Ala
NR_033969.1:n.856G>C (PLCE1-AS1)
XM_006717885.2:c.4726C>G (PLCE1)	XP_006717948.1:p.Pro1576Ala
XM_006717886.2:c.4726C>G (PLCE1)	XP_006717949.1:p.Pro1576Ala
XM_006717888.2:c.4726C>G (PLCE1)	XP_006717951.1:p.Pro1576Ala
XM_006717889.2:c.4678C>G (PLCE1)	XP_006717952.1:p.Pro1560Ala
XM_006717890.1:c.3802C>G (PLCE1)	XP_006717953.1:p.Pro1268Ala
XM_011539849.1:c.4726C>G (PLCE1)	XP_011538151.1:p.Pro1576Ala
XM_011539850.1:c.3571C>G (PLCE1)	XP_011538152.1:p.Pro1191Ala
XM_011539851.1:c.4726C>G (PLCE1)	XP_011538153.1:p.Pro1576Ala
XM_011539852.1:c.4726C>G (PLCE1)	XP_011538154.1:p.Pro1576Ala
XM_006717885.4:c.4726C>G (PLCE1)	XP_006717948.1:p.Pro1576Ala
XM_006717888.4:c.4726C>G (PLCE1)	XP_006717951.1:p.Pro1576Ala
XM_006717889.4:c.4678C>G (PLCE1)	XP_006717952.1:p.Pro1560Ala
XM_006717890.3:c.3802C>G (PLCE1)	XP_006717953.1:p.Pro1268Ala
XM_011539849.3:c.4726C>G (PLCE1)	XP_011538151.1:p.Pro1576Ala
XM_011539850.3:c.3571C>G (PLCE1)	XP_011538152.1:p.Pro1191Ala
XM_011539851.3:c.4726C>G (PLCE1)	XP_011538153.1:p.Pro1576Ala
XM_011539852.3:c.4726C>G (PLCE1)	XP_011538154.1:p.Pro1576Ala
XM_017016310.2:c.4726C>G (PLCE1)	XP_016871799.1:p.Pro1576Ala
XM_017016311.2:c.4726C>G (PLCE1)	XP_016871800.1:p.Pro1576Ala
XM_017016312.2:c.3754C>G (PLCE1)	XP_016871801.1:p.Pro1252Ala
NM_001288989.2:c.4678C>G (PLCE1)	NP_001275918.1:p.Pro1560Ala
NM_016341.4:c.4726C>G (PLCE1) MANE Select	NP_057425.3:p.Pro1576Ala