Canonical Allele Identifier: CA2610242129

Gene: PLCE1 NOC3L

Linked Data

• gnomAD v4: 10-94328111-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94328111C>T , CM000672.2:g.94328111C>T	GRCh38
NC_000010.10:g.96087868C>T , CM000672.1:g.96087868C>T	GRCh37
NC_000010.9:g.96077858C>T	NCBI36
NG_015799.1:g.339123C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371375.2:c.9016C>T (PLCE1)	ENSP00000360426.1:n.9016C>T
ENST00000688810.1:c.6105C>T (PLCE1)	ENSP00000509140.1:n.6105C>T
ENST00000690340.1:n.4721C>T (PLCE1)
ENST00000692396.1:c.*168C>T (PLCE1)	ENSP00000508605.1:n.*168C>T
ENST00000371380.8:c.*168C>T (PLCE1) MANE Select	ENSP00000360431.2:n.*168C>T
ENST00000371385.8:c.*168C>T (PLCE1)	ENSP00000360438.4:n.*168C>T
ENST00000675218.1:c.6153C>T (PLCE1)	ENSP00000501910.1:n.6153C>T
ENST00000675487.1:c.*3010C>T (PLCE1)	ENSP00000502340.1:n.*3010C>T
ENST00000260766.7:c.*168C>T (PLCE1)	ENSP00000260766.3:n.*168C>T
ENST00000371380.7:c.*168C>T (PLCE1)	ENSP00000360431.2:n.*168C>T
ENST00000371385.7:c.*168C>T (PLCE1)	ENSP00000360438.3:n.*168C>T
NM_001165979.2:c.*168C>T (PLCE1)	NP_001159451.1:n.*168C>T
NM_001288989.1:c.*168C>T (PLCE1)	NP_001275918.1:n.*168C>T
NM_016341.3:c.*168C>T (PLCE1)	NP_057425.3:n.*168C>T
XM_006717885.2:c.*168C>T (PLCE1)	XP_006717948.1:n.*168C>T
XM_006717888.2:c.*168C>T (PLCE1)	XP_006717951.1:n.*168C>T
XM_006717889.2:c.*168C>T (PLCE1)	XP_006717952.1:n.*168C>T
XM_006717890.1:c.*168C>T (PLCE1)	XP_006717953.1:n.*168C>T
XM_011539849.1:c.*168C>T (PLCE1)	XP_011538151.1:n.*168C>T
XM_011539850.1:c.*168C>T (PLCE1)	XP_011538152.1:n.*168C>T
XR_945799.1:n.3310+5279G>A (NOC3L)
XM_006717885.4:c.*168C>T (PLCE1)	XP_006717948.1:n.*168C>T
XM_006717888.4:c.*168C>T (PLCE1)	XP_006717951.1:n.*168C>T
XM_006717889.4:c.*168C>T (PLCE1)	XP_006717952.1:n.*168C>T
XM_006717890.3:c.*168C>T (PLCE1)	XP_006717953.1:n.*168C>T
XM_011539849.3:c.*168C>T (PLCE1)	XP_011538151.1:n.*168C>T
XM_011539850.3:c.*168C>T (PLCE1)	XP_011538152.1:n.*168C>T
XM_017016310.2:c.*168C>T (PLCE1)	XP_016871799.1:n.*168C>T
XM_017016312.2:c.*168C>T (PLCE1)	XP_016871801.1:n.*168C>T
XR_002957007.1:n.3311+5279G>A (NOC3L)
NM_001288989.2:c.*168C>T (PLCE1)	NP_001275918.1:n.*168C>T
NM_016341.4:c.*168C>T (PLCE1) MANE Select	NP_057425.3:n.*168C>T