Canonical Allele Identifier: CA595299956

Gene: PLCE1 NOC3L

Linked Data

• dbSNP Id: rs1424471445
• gnomAD v2: 10-96087834-CAT-C
• gnomAD v3: 10-94328077-CAT-C
• gnomAD v4: 10-94328077-CAT-C
• MyVariant Identifiers: chr10:g.96087835_96087836del (hg19) ; chr10:g.94328078_94328079del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94328078_94328079del , CM000672.2:g.94328078_94328079del	GRCh38
NC_000010.10:g.96087835_96087836del , CM000672.1:g.96087835_96087836del	GRCh37
NC_000010.9:g.96077825_96077826del	NCBI36
NG_015799.1:g.339090_339091del

Transcript Alleles

HGVS	Amino-acid change
ENST00000371375.2:c.8983_8984del (PLCE1)	ENSP00000360426.1:n.8983_8984del
ENST00000688810.1:c.6072_6073del (PLCE1)	ENSP00000509140.1:n.6072_6073del
ENST00000690340.1:n.4688_4689del (PLCE1)
ENST00000692396.1:c.*135_*136del (PLCE1)	ENSP00000508605.1:n.*135_*136del
ENST00000371380.8:c.*135_*136del (PLCE1) MANE Select	ENSP00000360431.2:n.*135_*136del
ENST00000371385.8:c.*135_*136del (PLCE1)	ENSP00000360438.4:n.*135_*136del
ENST00000675218.1:c.6120_6121del (PLCE1)	ENSP00000501910.1:n.6120_6121del
ENST00000675487.1:c.*2977_*2978del (PLCE1)	ENSP00000502340.1:n.*2977_*2978del
ENST00000260766.7:c.*135_*136del (PLCE1)	ENSP00000260766.3:n.*135_*136del
ENST00000371380.7:c.*135_*136del (PLCE1)	ENSP00000360431.2:n.*135_*136del
ENST00000371385.7:c.*135_*136del (PLCE1)	ENSP00000360438.3:n.*135_*136del
NM_001165979.2:c.*135_*136del (PLCE1)	NP_001159451.1:n.*135_*136del
NM_001288989.1:c.*135_*136del (PLCE1)	NP_001275918.1:n.*135_*136del
NM_016341.3:c.*135_*136del (PLCE1)	NP_057425.3:n.*135_*136del
XM_006717885.2:c.*135_*136del (PLCE1)	XP_006717948.1:n.*135_*136del
XM_006717888.2:c.*135_*136del (PLCE1)	XP_006717951.1:n.*135_*136del
XM_006717889.2:c.*135_*136del (PLCE1)	XP_006717952.1:n.*135_*136del
XM_006717890.1:c.*135_*136del (PLCE1)	XP_006717953.1:n.*135_*136del
XM_011539849.1:c.*135_*136del (PLCE1)	XP_011538151.1:n.*135_*136del
XM_011539850.1:c.*135_*136del (PLCE1)	XP_011538152.1:n.*135_*136del
XR_945799.1:n.3310+5311_3310+5312del (NOC3L)
XM_006717885.4:c.*135_*136del (PLCE1)	XP_006717948.1:n.*135_*136del
XM_006717888.4:c.*135_*136del (PLCE1)	XP_006717951.1:n.*135_*136del
XM_006717889.4:c.*135_*136del (PLCE1)	XP_006717952.1:n.*135_*136del
XM_006717890.3:c.*135_*136del (PLCE1)	XP_006717953.1:n.*135_*136del
XM_011539849.3:c.*135_*136del (PLCE1)	XP_011538151.1:n.*135_*136del
XM_011539850.3:c.*135_*136del (PLCE1)	XP_011538152.1:n.*135_*136del
XM_017016310.2:c.*135_*136del (PLCE1)	XP_016871799.1:n.*135_*136del
XM_017016312.2:c.*135_*136del (PLCE1)	XP_016871801.1:n.*135_*136del
XR_002957007.1:n.3311+5311_3311+5312del (NOC3L)
NM_001288989.2:c.*135_*136del (PLCE1)	NP_001275918.1:n.*135_*136del
NM_016341.4:c.*135_*136del (PLCE1) MANE Select	NP_057425.3:n.*135_*136del