Canonical Allele Identifier: CA2574617678

Gene: PLCE1

Linked Data

• gnomAD v4: 10-94270461-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94270463del , CM000672.2:g.94270463del	GRCh38
NC_000010.10:g.96030220del , CM000672.1:g.96030220del	GRCh37
NC_000010.9:g.96020210del	NCBI36
NG_015799.1:g.281475del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.3466-23del	ENSP00000360426.1:n.3466-23del
ENST00000685253.1:c.*933-23del	ENSP00000509405.1:n.*933-23del
ENST00000685889.1:n.1125-23del
ENST00000686954.1:c.4390-23del	ENSP00000508416.1:n.4390-23del
ENST00000688810.1:c.3418-23del	ENSP00000509140.1:n.3418-23del
ENST00000689233.1:n.4720-23del
ENST00000692286.1:c.4390-23del	ENSP00000509490.1:n.4390-23del
ENST00000692396.1:c.4342-23del	ENSP00000508605.1:n.4342-23del
ENST00000371380.8:c.4390-23del MANE Select	ENSP00000360431.2:n.4390-23del
ENST00000371385.8:c.3364-23del	ENSP00000360438.4:n.3364-23del
ENST00000674738.1:c.2795-23del
ENST00000674827.1:c.2467-23del	ENSP00000502523.1:n.2467-23del
ENST00000675218.1:c.3466-23del	ENSP00000501910.1:n.3466-23del
ENST00000675487.1:c.*323-23del	ENSP00000502340.1:n.*323-23del
ENST00000675718.1:c.3617-23del
ENST00000676102.1:c.3235-23del	ENSP00000502811.1:n.3235-23del
ENST00000260766.7:c.4390-23del	ENSP00000260766.3:n.4390-23del
ENST00000371375.1:c.3466-23del	ENSP00000360426.1:n.3466-23del
ENST00000371380.7:c.4390-23del	ENSP00000360431.2:n.4390-23del
ENST00000371385.7:c.3466-23del	ENSP00000360438.3:n.3466-23del
NM_001165979.2:c.3466-23del	NP_001159451.1:n.3466-23del
NM_001288989.1:c.4342-23del	NP_001275918.1:n.4342-23del
NM_016341.3:c.4390-23del	NP_057425.3:n.4390-23del
XM_006717885.2:c.4390-23del	XP_006717948.1:n.4390-23del
XM_006717886.2:c.4390-23del	XP_006717949.1:n.4390-23del
XM_006717888.2:c.4390-23del	XP_006717951.1:n.4390-23del
XM_006717889.2:c.4342-23del	XP_006717952.1:n.4342-23del
XM_006717890.1:c.3466-23del	XP_006717953.1:n.3466-23del
XM_011539849.1:c.4390-23del	XP_011538151.1:n.4390-23del
XM_011539850.1:c.3235-23del	XP_011538152.1:n.3235-23del
XM_011539851.1:c.4390-23del	XP_011538153.1:n.4390-23del
XM_011539852.1:c.4390-23del	XP_011538154.1:n.4390-23del
XM_006717885.4:c.4390-23del	XP_006717948.1:n.4390-23del
XM_006717888.4:c.4390-23del	XP_006717951.1:n.4390-23del
XM_006717889.4:c.4342-23del	XP_006717952.1:n.4342-23del
XM_006717890.3:c.3466-23del	XP_006717953.1:n.3466-23del
XM_011539849.3:c.4390-23del	XP_011538151.1:n.4390-23del
XM_011539850.3:c.3235-23del	XP_011538152.1:n.3235-23del
XM_011539851.3:c.4390-23del	XP_011538153.1:n.4390-23del
XM_011539852.3:c.4390-23del	XP_011538154.1:n.4390-23del
XM_017016310.2:c.4390-23del	XP_016871799.1:n.4390-23del
XM_017016311.2:c.4390-23del	XP_016871800.1:n.4390-23del
XM_017016312.2:c.3418-23del	XP_016871801.1:n.3418-23del
NM_001288989.2:c.4342-23del	NP_001275918.1:n.4342-23del
NM_016341.4:c.4390-23del MANE Select	NP_057425.3:n.4390-23del