Canonical Allele Identifier: CA377648608

Gene: PLCE1 NOC3L

Linked Data

• MyVariant Identifiers: chr10:g.96081802G>T (hg19) ; chr10:g.94322045G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94322045G>T , CM000672.2:g.94322045G>T	GRCh38
NC_000010.10:g.96081802G>T , CM000672.1:g.96081802G>T	GRCh37
NC_000010.9:g.96071792G>T	NCBI36
NG_015799.1:g.333057G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.5563G>T (PLCE1)	ENSP00000360426.1:p.Asp1855Tyr
ENST00000685253.1:c.*3030G>T (PLCE1)	ENSP00000509405.1:n.*3030G>T
ENST00000685889.1:n.3222G>T (PLCE1)
ENST00000686807.1:n.1906G>T (PLCE1)
ENST00000686954.1:c.*1771G>T (PLCE1)	ENSP00000508416.1:n.*1771G>T
ENST00000688810.1:c.5515G>T (PLCE1)	ENSP00000509140.1:p.Asp1839Tyr
ENST00000689233.1:n.10695G>T (PLCE1)
ENST00000690340.1:n.4160G>T (PLCE1)
ENST00000692286.1:c.6355G>T (PLCE1)	ENSP00000509490.1:p.Asp2119Tyr
ENST00000692396.1:c.6439G>T (PLCE1)	ENSP00000508605.1:p.Asp2147Tyr
ENST00000371380.8:c.6487G>T (PLCE1) MANE Select	ENSP00000360431.2:p.Asp2163Tyr
ENST00000371385.8:c.5461G>T (PLCE1)	ENSP00000360438.4:p.Asp1821Tyr
ENST00000675218.1:c.5563G>T (PLCE1)	ENSP00000501910.1:p.Asp1855Tyr
ENST00000675487.1:c.*2420G>T (PLCE1)	ENSP00000502340.1:n.*2420G>T
ENST00000260766.7:c.6487G>T (PLCE1)	ENSP00000260766.3:p.Asp2163Tyr
ENST00000371375.1:c.5563G>T (PLCE1)	ENSP00000360426.1:p.Asp1855Tyr
ENST00000371380.7:c.6487G>T (PLCE1)	ENSP00000360431.2:p.Asp2163Tyr
ENST00000371385.7:c.5563G>T (PLCE1)	ENSP00000360438.3:p.Asp1855Tyr
NM_001165979.2:c.5563G>T (PLCE1)	NP_001159451.1:p.Asp1855Tyr
NM_001288989.1:c.6439G>T (PLCE1)	NP_001275918.1:p.Asp2147Tyr
NM_016341.3:c.6487G>T (PLCE1)	NP_057425.3:p.Asp2163Tyr
XM_006717885.2:c.6529G>T (PLCE1)	XP_006717948.1:p.Asp2177Tyr
XM_006717886.2:c.6529G>T (PLCE1)	XP_006717949.1:p.Asp2177Tyr
XM_006717888.2:c.6526G>T (PLCE1)	XP_006717951.1:p.Asp2176Tyr
XM_006717889.2:c.6481G>T (PLCE1)	XP_006717952.1:p.Asp2161Tyr
XM_006717890.1:c.5605G>T (PLCE1)	XP_006717953.1:p.Asp1869Tyr
XM_011539849.1:c.6529G>T (PLCE1)	XP_011538151.1:p.Asp2177Tyr
XM_011539850.1:c.5374G>T (PLCE1)	XP_011538152.1:p.Asp1792Tyr
XR_945799.1:n.3311-6581C>A (NOC3L)
XM_006717885.4:c.6529G>T (PLCE1)	XP_006717948.1:p.Asp2177Tyr
XM_006717888.4:c.6526G>T (PLCE1)	XP_006717951.1:p.Asp2176Tyr
XM_006717889.4:c.6481G>T (PLCE1)	XP_006717952.1:p.Asp2161Tyr
XM_006717890.3:c.5605G>T (PLCE1)	XP_006717953.1:p.Asp1869Tyr
XM_011539849.3:c.6529G>T (PLCE1)	XP_011538151.1:p.Asp2177Tyr
XM_011539850.3:c.5374G>T (PLCE1)	XP_011538152.1:p.Asp1792Tyr
XM_017016310.2:c.6529G>T (PLCE1)	XP_016871799.1:p.Asp2177Tyr
XM_017016311.2:c.6529G>T (PLCE1)	XP_016871800.1:p.Asp2177Tyr
XM_017016312.2:c.5515G>T (PLCE1)	XP_016871801.1:p.Asp1839Tyr
XR_002957007.1:n.3312-6581C>A (NOC3L)
NM_001288989.2:c.6439G>T (PLCE1)	NP_001275918.1:p.Asp2147Tyr
NM_016341.4:c.6487G>T (PLCE1) MANE Select	NP_057425.3:p.Asp2163Tyr