Canonical Allele Identifier: CA470986218

Gene: PLCE1

Linked Data

• MyVariant Identifiers: chr10:g.96058422T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298665T>G , CM000672.2:g.94298665T>G	GRCh38
NC_000010.10:g.96058422T>G , CM000672.1:g.96058422T>G	GRCh37
NC_000010.9:g.96048412T>G	NCBI36
NG_015799.1:g.309677T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.4530T>G	ENSP00000360426.1:p.Thr1510=
ENST00000685253.1:c.*1997T>G	ENSP00000509405.1:n.*1997T>G
ENST00000685889.1:n.2189T>G
ENST00000686807.1:n.873T>G
ENST00000686954.1:c.*738T>G	ENSP00000508416.1:n.*738T>G
ENST00000688810.1:c.4482T>G	ENSP00000509140.1:p.Thr1494=
ENST00000689233.1:n.9662T>G
ENST00000690340.1:n.3127T>G
ENST00000692286.1:c.5322T>G	ENSP00000509490.1:p.Thr1774=
ENST00000692396.1:c.5406T>G	ENSP00000508605.1:p.Thr1802=
ENST00000371380.8:c.5454T>G MANE Select	ENSP00000360431.2:p.Thr1818=
ENST00000371385.8:c.4428T>G	ENSP00000360438.4:p.Thr1476=
ENST00000674738.1:c.4009T>G
ENST00000674827.1:c.3570T>G	ENSP00000502523.1:p.Thr1190=
ENST00000675218.1:c.4530T>G	ENSP00000501910.1:p.Thr1510=
ENST00000675487.1:c.*1387T>G	ENSP00000502340.1:n.*1387T>G
ENST00000675718.1:c.4723T>G
ENST00000260766.7:c.5454T>G	ENSP00000260766.3:p.Thr1818=
ENST00000371375.1:c.4530T>G	ENSP00000360426.1:p.Thr1510=
ENST00000371380.7:c.5454T>G	ENSP00000360431.2:p.Thr1818=
ENST00000371385.7:c.4530T>G	ENSP00000360438.3:p.Thr1510=
NM_001165979.2:c.4530T>G	NP_001159451.1:p.Thr1510=
NM_001288989.1:c.5406T>G	NP_001275918.1:p.Thr1802=
NM_016341.3:c.5454T>G	NP_057425.3:p.Thr1818=
XM_006717885.2:c.5496T>G	XP_006717948.1:p.Thr1832=
XM_006717886.2:c.5496T>G	XP_006717949.1:p.Thr1832=
XM_006717888.2:c.5493T>G	XP_006717951.1:p.Thr1831=
XM_006717889.2:c.5448T>G	XP_006717952.1:p.Thr1816=
XM_006717890.1:c.4572T>G	XP_006717953.1:p.Thr1524=
XM_011539849.1:c.5496T>G	XP_011538151.1:p.Thr1832=
XM_011539850.1:c.4341T>G	XP_011538152.1:p.Thr1447=
XM_006717885.4:c.5496T>G	XP_006717948.1:p.Thr1832=
XM_006717888.4:c.5493T>G	XP_006717951.1:p.Thr1831=
XM_006717889.4:c.5448T>G	XP_006717952.1:p.Thr1816=
XM_006717890.3:c.4572T>G	XP_006717953.1:p.Thr1524=
XM_011539849.3:c.5496T>G	XP_011538151.1:p.Thr1832=
XM_011539850.3:c.4341T>G	XP_011538152.1:p.Thr1447=
XM_017016310.2:c.5496T>G	XP_016871799.1:p.Thr1832=
XM_017016311.2:c.5496T>G	XP_016871800.1:p.Thr1832=
XM_017016312.2:c.4482T>G	XP_016871801.1:p.Thr1494=
NM_001288989.2:c.5406T>G	NP_001275918.1:p.Thr1802=
NM_016341.4:c.5454T>G MANE Select	NP_057425.3:p.Thr1818=