Canonical Allele Identifier: CA470986595

Gene: PLCE1

Linked Data

• MyVariant Identifiers: chr10:g.96058341C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298584C>G , CM000672.2:g.94298584C>G	GRCh38
NC_000010.10:g.96058341C>G , CM000672.1:g.96058341C>G	GRCh37
NC_000010.9:g.96048331C>G	NCBI36
NG_015799.1:g.309596C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000371375.2:c.4449C>G	ENSP00000360426.1:p.Ala1483=
ENST00000685253.1:c.*1916C>G	ENSP00000509405.1:n.*1916C>G
ENST00000685889.1:n.2108C>G
ENST00000686807.1:n.792C>G
ENST00000686954.1:c.*657C>G	ENSP00000508416.1:n.*657C>G
ENST00000688810.1:c.4401C>G	ENSP00000509140.1:p.Ala1467=
ENST00000689233.1:n.9581C>G
ENST00000690340.1:n.3046C>G
ENST00000692286.1:c.5241C>G	ENSP00000509490.1:p.Ala1747=
ENST00000692396.1:c.5325C>G	ENSP00000508605.1:p.Ala1775=
ENST00000371380.8:c.5373C>G MANE Select	ENSP00000360431.2:p.Ala1791=
ENST00000371385.8:c.4347C>G	ENSP00000360438.4:p.Ala1449=
ENST00000674738.1:c.3928C>G
ENST00000674827.1:c.3489C>G	ENSP00000502523.1:p.Ala1163=
ENST00000675218.1:c.4449C>G	ENSP00000501910.1:p.Ala1483=
ENST00000675487.1:c.*1306C>G	ENSP00000502340.1:n.*1306C>G
ENST00000675718.1:c.4642C>G
ENST00000260766.7:c.5373C>G	ENSP00000260766.3:p.Ala1791=
ENST00000371375.1:c.4449C>G	ENSP00000360426.1:p.Ala1483=
ENST00000371380.7:c.5373C>G	ENSP00000360431.2:p.Ala1791=
ENST00000371385.7:c.4449C>G	ENSP00000360438.3:p.Ala1483=
NM_001165979.2:c.4449C>G	NP_001159451.1:p.Ala1483=
NM_001288989.1:c.5325C>G	NP_001275918.1:p.Ala1775=
NM_016341.3:c.5373C>G	NP_057425.3:p.Ala1791=
XM_006717885.2:c.5415C>G	XP_006717948.1:p.Ala1805=
XM_006717886.2:c.5415C>G	XP_006717949.1:p.Ala1805=
XM_006717888.2:c.5412C>G	XP_006717951.1:p.Ala1804=
XM_006717889.2:c.5367C>G	XP_006717952.1:p.Ala1789=
XM_006717890.1:c.4491C>G	XP_006717953.1:p.Ala1497=
XM_011539849.1:c.5415C>G	XP_011538151.1:p.Ala1805=
XM_011539850.1:c.4260C>G	XP_011538152.1:p.Ala1420=
XM_006717885.4:c.5415C>G	XP_006717948.1:p.Ala1805=
XM_006717888.4:c.5412C>G	XP_006717951.1:p.Ala1804=
XM_006717889.4:c.5367C>G	XP_006717952.1:p.Ala1789=
XM_006717890.3:c.4491C>G	XP_006717953.1:p.Ala1497=
XM_011539849.3:c.5415C>G	XP_011538151.1:p.Ala1805=
XM_011539850.3:c.4260C>G	XP_011538152.1:p.Ala1420=
XM_017016310.2:c.5415C>G	XP_016871799.1:p.Ala1805=
XM_017016311.2:c.5415C>G	XP_016871800.1:p.Ala1805=
XM_017016312.2:c.4401C>G	XP_016871801.1:p.Ala1467=
NM_001288989.2:c.5325C>G	NP_001275918.1:p.Ala1775=
NM_016341.4:c.5373C>G MANE Select	NP_057425.3:p.Ala1791=