Canonical Allele Identifier: CA1928927614

Gene: PLCE1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94132444C= , CM000672.2:g.94132444C=	GRCh38
NC_000010.10:g.95892201C= , CM000672.1:g.95892201C=	GRCh37
NC_000010.9:g.95882191C=	NCBI36
NG_015799.1:g.143456C=

Transcript Alleles

HGVS	Amino-acid Change
NM_016341.4:c.1477C= MANE Select	NP_057425.3:p.Arg493=
ENST00000371380.8:c.1477C= MANE Select	ENSP00000360431.2:p.Arg493=
NM_001165979.2:c.553C=	NP_001159451.1:p.Arg185=
NM_001288989.1:c.1477C=	NP_001275918.1:p.Arg493=
NM_001288989.2:c.1477C=	NP_001275918.1:p.Arg493=
NM_016341.3:c.1477C=	NP_057425.3:p.Arg493=
ENST00000260766.7:c.1477C=	ENSP00000260766.3:p.Arg493=
ENST00000371375.1:c.553C=	ENSP00000360426.1:p.Arg185=
ENST00000371375.2:c.553C=	ENSP00000360426.1:p.Arg185=
ENST00000371380.7:c.1477C=	ENSP00000360431.2:p.Arg493=
ENST00000371385.7:c.553C=	ENSP00000360438.3:p.Arg185=
ENST00000371385.8:c.553C=	ENSP00000360438.4:p.Arg185=
ENST00000675218.1:c.553C=	ENSP00000501910.1:p.Arg185=
ENST00000675487.1:c.1477C=	ENSP00000502340.1:p.Arg493=
ENST00000675718.1:c.548C=
ENST00000676102.1:c.322C=	ENSP00000502811.1:p.Arg108=
ENST00000685253.1:c.1477C=	ENSP00000509405.1:p.Arg493=
ENST00000686954.1:c.1477C=	ENSP00000508416.1:p.Arg493=
ENST00000688810.1:c.553C=	ENSP00000509140.1:p.Arg185=
ENST00000689233.1:n.1807C=
ENST00000689699.1:n.1807C=
ENST00000689982.1:n.556C=
ENST00000692286.1:c.1477C=	ENSP00000509490.1:p.Arg493=
ENST00000692396.1:c.1477C=	ENSP00000508605.1:p.Arg493=
XM_006717885.2:c.1477C=	XP_006717948.1:p.Arg493=
XM_006717885.4:c.1477C=	XP_006717948.1:p.Arg493=
XM_006717886.2:c.1477C=	XP_006717949.1:p.Arg493=
XM_006717888.2:c.1477C=	XP_006717951.1:p.Arg493=
XM_006717888.4:c.1477C=	XP_006717951.1:p.Arg493=
XM_006717889.2:c.1477C=	XP_006717952.1:p.Arg493=
XM_006717889.4:c.1477C=	XP_006717952.1:p.Arg493=
XM_006717890.1:c.553C=	XP_006717953.1:p.Arg185=
XM_006717890.3:c.553C=	XP_006717953.1:p.Arg185=
XM_011539849.1:c.1477C=	XP_011538151.1:p.Arg493=
XM_011539849.3:c.1477C=	XP_011538151.1:p.Arg493=
XM_011539850.1:c.322C=	XP_011538152.1:p.Arg108=
XM_011539850.3:c.322C=	XP_011538152.1:p.Arg108=
XM_011539851.1:c.1477C=	XP_011538153.1:p.Arg493=
XM_011539851.3:c.1477C=	XP_011538153.1:p.Arg493=
XM_011539852.1:c.1477C=	XP_011538154.1:p.Arg493=
XM_011539852.3:c.1477C=	XP_011538154.1:p.Arg493=
XM_017016310.2:c.1477C=	XP_016871799.1:p.Arg493=
XM_017016311.2:c.1477C=	XP_016871800.1:p.Arg493=
XM_017016312.2:c.553C=	XP_016871801.1:p.Arg185=