Canonical Allele Identifier: CA470986199

Gene: PLCE1

Linked Data

• MyVariant Identifiers: chr10:g.96058407A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298650A>T , CM000672.2:g.94298650A>T	GRCh38
NC_000010.10:g.96058407A>T , CM000672.1:g.96058407A>T	GRCh37
NC_000010.9:g.96048397A>T	NCBI36
NG_015799.1:g.309662A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.4515A>T	ENSP00000360426.1:p.Ala1505=
ENST00000685253.1:c.*1982A>T	ENSP00000509405.1:n.*1982A>T
ENST00000685889.1:n.2174A>T
ENST00000686807.1:n.858A>T
ENST00000686954.1:c.*723A>T	ENSP00000508416.1:n.*723A>T
ENST00000688810.1:c.4467A>T	ENSP00000509140.1:p.Ala1489=
ENST00000689233.1:n.9647A>T
ENST00000690340.1:n.3112A>T
ENST00000692286.1:c.5307A>T	ENSP00000509490.1:p.Ala1769=
ENST00000692396.1:c.5391A>T	ENSP00000508605.1:p.Ala1797=
ENST00000371380.8:c.5439A>T MANE Select	ENSP00000360431.2:p.Ala1813=
ENST00000371385.8:c.4413A>T	ENSP00000360438.4:p.Ala1471=
ENST00000674738.1:c.3994A>T
ENST00000674827.1:c.3555A>T	ENSP00000502523.1:p.Ala1185=
ENST00000675218.1:c.4515A>T	ENSP00000501910.1:p.Ala1505=
ENST00000675487.1:c.*1372A>T	ENSP00000502340.1:n.*1372A>T
ENST00000675718.1:c.4708A>T
ENST00000260766.7:c.5439A>T	ENSP00000260766.3:p.Ala1813=
ENST00000371375.1:c.4515A>T	ENSP00000360426.1:p.Ala1505=
ENST00000371380.7:c.5439A>T	ENSP00000360431.2:p.Ala1813=
ENST00000371385.7:c.4515A>T	ENSP00000360438.3:p.Ala1505=
NM_001165979.2:c.4515A>T	NP_001159451.1:p.Ala1505=
NM_001288989.1:c.5391A>T	NP_001275918.1:p.Ala1797=
NM_016341.3:c.5439A>T	NP_057425.3:p.Ala1813=
XM_006717885.2:c.5481A>T	XP_006717948.1:p.Ala1827=
XM_006717886.2:c.5481A>T	XP_006717949.1:p.Ala1827=
XM_006717888.2:c.5478A>T	XP_006717951.1:p.Ala1826=
XM_006717889.2:c.5433A>T	XP_006717952.1:p.Ala1811=
XM_006717890.1:c.4557A>T	XP_006717953.1:p.Ala1519=
XM_011539849.1:c.5481A>T	XP_011538151.1:p.Ala1827=
XM_011539850.1:c.4326A>T	XP_011538152.1:p.Ala1442=
XM_006717885.4:c.5481A>T	XP_006717948.1:p.Ala1827=
XM_006717888.4:c.5478A>T	XP_006717951.1:p.Ala1826=
XM_006717889.4:c.5433A>T	XP_006717952.1:p.Ala1811=
XM_006717890.3:c.4557A>T	XP_006717953.1:p.Ala1519=
XM_011539849.3:c.5481A>T	XP_011538151.1:p.Ala1827=
XM_011539850.3:c.4326A>T	XP_011538152.1:p.Ala1442=
XM_017016310.2:c.5481A>T	XP_016871799.1:p.Ala1827=
XM_017016311.2:c.5481A>T	XP_016871800.1:p.Ala1827=
XM_017016312.2:c.4467A>T	XP_016871801.1:p.Ala1489=
NM_001288989.2:c.5391A>T	NP_001275918.1:p.Ala1797=
NM_016341.4:c.5439A>T MANE Select	NP_057425.3:p.Ala1813=