Canonical Allele Identifier: CA377640938

Gene: PLCE1

Linked Data

• MyVariant Identifiers: chr10:g.96053384A>G (hg19) ; chr10:g.94293627A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94293627A>G , CM000672.2:g.94293627A>G	GRCh38
NC_000010.10:g.96053384A>G , CM000672.1:g.96053384A>G	GRCh37
NC_000010.9:g.96043374A>G	NCBI36
NG_015799.1:g.304639A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.4231A>G	ENSP00000360426.1:p.Thr1411Ala
ENST00000685253.1:c.*1698A>G	ENSP00000509405.1:n.*1698A>G
ENST00000685889.1:n.1890A>G
ENST00000686807.1:n.574A>G
ENST00000686954.1:c.*439A>G	ENSP00000508416.1:n.*439A>G
ENST00000688810.1:c.4183A>G	ENSP00000509140.1:p.Thr1395Ala
ENST00000689233.1:n.9363A>G
ENST00000690340.1:n.2828A>G
ENST00000692286.1:c.5036-4752A>G	ENSP00000509490.1:n.5036-4752A>G
ENST00000692396.1:c.5107A>G	ENSP00000508605.1:p.Thr1703Ala
ENST00000371380.8:c.5155A>G MANE Select	ENSP00000360431.2:p.Thr1719Ala
ENST00000371385.8:c.4129A>G	ENSP00000360438.4:p.Thr1377Ala
ENST00000674738.1:c.3710A>G
ENST00000674827.1:c.3271A>G	ENSP00000502523.1:p.Thr1091Ala
ENST00000675218.1:c.4231A>G	ENSP00000501910.1:p.Thr1411Ala
ENST00000675487.1:c.*1088A>G	ENSP00000502340.1:n.*1088A>G
ENST00000675718.1:c.4424A>G
ENST00000676102.1:c.4000A>G	ENSP00000502811.1:p.Thr1334Ala
ENST00000260766.7:c.5155A>G	ENSP00000260766.3:p.Thr1719Ala
ENST00000371375.1:c.4231A>G	ENSP00000360426.1:p.Thr1411Ala
ENST00000371380.7:c.5155A>G	ENSP00000360431.2:p.Thr1719Ala
ENST00000371385.7:c.4231A>G	ENSP00000360438.3:p.Thr1411Ala
NM_001165979.2:c.4231A>G	NP_001159451.1:p.Thr1411Ala
NM_001288989.1:c.5107A>G	NP_001275918.1:p.Thr1703Ala
NM_016341.3:c.5155A>G	NP_057425.3:p.Thr1719Ala
XM_006717885.2:c.5197A>G	XP_006717948.1:p.Thr1733Ala
XM_006717886.2:c.5197A>G	XP_006717949.1:p.Thr1733Ala
XM_006717888.2:c.5194A>G	XP_006717951.1:p.Thr1732Ala
XM_006717889.2:c.5149A>G	XP_006717952.1:p.Thr1717Ala
XM_006717890.1:c.4273A>G	XP_006717953.1:p.Thr1425Ala
XM_011539849.1:c.5197A>G	XP_011538151.1:p.Thr1733Ala
XM_011539850.1:c.4042A>G	XP_011538152.1:p.Thr1348Ala
XM_006717885.4:c.5197A>G	XP_006717948.1:p.Thr1733Ala
XM_006717888.4:c.5194A>G	XP_006717951.1:p.Thr1732Ala
XM_006717889.4:c.5149A>G	XP_006717952.1:p.Thr1717Ala
XM_006717890.3:c.4273A>G	XP_006717953.1:p.Thr1425Ala
XM_011539849.3:c.5197A>G	XP_011538151.1:p.Thr1733Ala
XM_011539850.3:c.4042A>G	XP_011538152.1:p.Thr1348Ala
XM_017016310.2:c.5197A>G	XP_016871799.1:p.Thr1733Ala
XM_017016311.2:c.5197A>G	XP_016871800.1:p.Thr1733Ala
XM_017016312.2:c.4183A>G	XP_016871801.1:p.Thr1395Ala
NM_001288989.2:c.5107A>G	NP_001275918.1:p.Thr1703Ala
NM_016341.4:c.5155A>G MANE Select	NP_057425.3:p.Thr1719Ala