Canonical Allele Identifier: CA470815220

Gene: PLCE1 PLCE1-AS1

Linked Data

• gnomAD v4: 10-94279575-A-T
• MyVariant Identifiers: chr10:g.96039332A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94279575A>T , CM000672.2:g.94279575A>T	GRCh38
NC_000010.10:g.96039332A>T , CM000672.1:g.96039332A>T	GRCh37
NC_000010.9:g.96029322A>T	NCBI36
NG_015799.1:g.290587A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.3742-207A>T (PLCE1)	ENSP00000360426.1:n.3742-207A>T
ENST00000685253.1:c.*1209-207A>T (PLCE1)	ENSP00000509405.1:n.*1209-207A>T
ENST00000685889.1:n.1401-207A>T (PLCE1)
ENST00000686954.1:c.4666-207A>T (PLCE1)	ENSP00000508416.1:n.4666-207A>T
ENST00000688810.1:c.3694-207A>T (PLCE1)	ENSP00000509140.1:n.3694-207A>T
ENST00000689233.1:n.4996-207A>T (PLCE1)
ENST00000692286.1:c.4666-207A>T (PLCE1)	ENSP00000509490.1:n.4666-207A>T
ENST00000692396.1:c.4618-207A>T (PLCE1)	ENSP00000508605.1:n.4618-207A>T
ENST00000371380.8:c.4666-207A>T (PLCE1) MANE Select	ENSP00000360431.2:n.4666-207A>T
ENST00000371385.8:c.3640-207A>T (PLCE1)	ENSP00000360438.4:n.3640-207A>T
ENST00000674738.1:c.3071-207A>T (PLCE1)
ENST00000674827.1:c.2743-207A>T (PLCE1)	ENSP00000502523.1:n.2743-207A>T
ENST00000675218.1:c.3742-207A>T (PLCE1)	ENSP00000501910.1:n.3742-207A>T
ENST00000675487.1:c.*599-207A>T (PLCE1)	ENSP00000502340.1:n.*599-207A>T
ENST00000675718.1:c.3893-207A>T (PLCE1)
ENST00000676102.1:c.3511-207A>T (PLCE1)	ENSP00000502811.1:n.3511-207A>T
ENST00000260766.7:c.4666-207A>T (PLCE1)	ENSP00000260766.3:n.4666-207A>T
ENST00000371375.1:c.3742-207A>T (PLCE1)	ENSP00000360426.1:n.3742-207A>T
ENST00000371380.7:c.4666-207A>T (PLCE1)	ENSP00000360431.2:n.4666-207A>T
ENST00000371385.7:c.3742-207A>T (PLCE1)	ENSP00000360438.3:n.3742-207A>T
NM_001165979.2:c.3742-207A>T (PLCE1)	NP_001159451.1:n.3742-207A>T
NM_001288989.1:c.4618-207A>T (PLCE1)	NP_001275918.1:n.4618-207A>T
NM_016341.3:c.4666-207A>T (PLCE1)	NP_057425.3:n.4666-207A>T
NR_033969.1:n.1123T>A (PLCE1-AS1)
XM_006717885.2:c.4666-207A>T (PLCE1)	XP_006717948.1:n.4666-207A>T
XM_006717886.2:c.4666-207A>T (PLCE1)	XP_006717949.1:n.4666-207A>T
XM_006717888.2:c.4666-207A>T (PLCE1)	XP_006717951.1:n.4666-207A>T
XM_006717889.2:c.4618-207A>T (PLCE1)	XP_006717952.1:n.4618-207A>T
XM_006717890.1:c.3742-207A>T (PLCE1)	XP_006717953.1:n.3742-207A>T
XM_011539849.1:c.4666-207A>T (PLCE1)	XP_011538151.1:n.4666-207A>T
XM_011539850.1:c.3511-207A>T (PLCE1)	XP_011538152.1:n.3511-207A>T
XM_011539851.1:c.4666-207A>T (PLCE1)	XP_011538153.1:n.4666-207A>T
XM_011539852.1:c.4666-207A>T (PLCE1)	XP_011538154.1:n.4666-207A>T
XM_006717885.4:c.4666-207A>T (PLCE1)	XP_006717948.1:n.4666-207A>T
XM_006717888.4:c.4666-207A>T (PLCE1)	XP_006717951.1:n.4666-207A>T
XM_006717889.4:c.4618-207A>T (PLCE1)	XP_006717952.1:n.4618-207A>T
XM_006717890.3:c.3742-207A>T (PLCE1)	XP_006717953.1:n.3742-207A>T
XM_011539849.3:c.4666-207A>T (PLCE1)	XP_011538151.1:n.4666-207A>T
XM_011539850.3:c.3511-207A>T (PLCE1)	XP_011538152.1:n.3511-207A>T
XM_011539851.3:c.4666-207A>T (PLCE1)	XP_011538153.1:n.4666-207A>T
XM_011539852.3:c.4666-207A>T (PLCE1)	XP_011538154.1:n.4666-207A>T
XM_017016310.2:c.4666-207A>T (PLCE1)	XP_016871799.1:n.4666-207A>T
XM_017016311.2:c.4666-207A>T (PLCE1)	XP_016871800.1:n.4666-207A>T
XM_017016312.2:c.3694-207A>T (PLCE1)	XP_016871801.1:n.3694-207A>T
NM_001288989.2:c.4618-207A>T (PLCE1)	NP_001275918.1:n.4618-207A>T
NM_016341.4:c.4666-207A>T (PLCE1) MANE Select	NP_057425.3:n.4666-207A>T