Canonical Allele Identifier: CA1928987709

Gene: PLCE1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94270488_94270489delinsAG , CM000672.2:g.94270488_94270489delinsAG	GRCh38
NC_000010.10:g.96030245_96030246delinsAG , CM000672.1:g.96030245_96030246delinsAG	GRCh37
NC_000010.9:g.96020235_96020236delinsAG	NCBI36
NG_015799.1:g.281500_281501delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.3468_3469delinsAG	ENSP00000360426.1:p.Glu1156=
ENST00000685253.1:c.*935_*936delinsAG	ENSP00000509405.1:n.*935_*936delinsAG
ENST00000685889.1:n.1127_1128delinsAG
ENST00000686954.1:c.4392_4393delinsAG	ENSP00000508416.1:p.Glu1464=
ENST00000688810.1:c.3420_3421delinsAG	ENSP00000509140.1:p.Glu1140=
ENST00000689233.1:n.4722_4723delinsAG
ENST00000692286.1:c.4392_4393delinsAG	ENSP00000509490.1:p.Glu1464=
ENST00000692396.1:c.4344_4345delinsAG	ENSP00000508605.1:p.Glu1448=
ENST00000371380.8:c.4392_4393delinsAG MANE Select	ENSP00000360431.2:p.Glu1464=
ENST00000371385.8:c.3366_3367delinsAG	ENSP00000360438.4:p.Glu1122=
ENST00000674738.1:c.2797_2798delinsAG
ENST00000674827.1:c.2469_2470delinsAG	ENSP00000502523.1:p.Glu823=
ENST00000675218.1:c.3468_3469delinsAG	ENSP00000501910.1:p.Glu1156=
ENST00000675487.1:c.*325_*326delinsAG	ENSP00000502340.1:n.*325_*326delinsAG
ENST00000675718.1:c.3619_3620delinsAG
ENST00000676102.1:c.3237_3238delinsAG	ENSP00000502811.1:p.Glu1079=
ENST00000260766.7:c.4392_4393delinsAG	ENSP00000260766.3:p.Glu1464=
ENST00000371375.1:c.3468_3469delinsAG	ENSP00000360426.1:p.Glu1156=
ENST00000371380.7:c.4392_4393delinsAG	ENSP00000360431.2:p.Glu1464=
ENST00000371385.7:c.3468_3469delinsAG	ENSP00000360438.3:p.Glu1156=
NM_001165979.2:c.3468_3469delinsAG	NP_001159451.1:p.Glu1156=
NM_001288989.1:c.4344_4345delinsAG	NP_001275918.1:p.Glu1448=
NM_016341.3:c.4392_4393delinsAG	NP_057425.3:p.Glu1464=
XM_006717885.2:c.4392_4393delinsAG	XP_006717948.1:p.Glu1464=
XM_006717886.2:c.4392_4393delinsAG	XP_006717949.1:p.Glu1464=
XM_006717888.2:c.4392_4393delinsAG	XP_006717951.1:p.Glu1464=
XM_006717889.2:c.4344_4345delinsAG	XP_006717952.1:p.Glu1448=
XM_006717890.1:c.3468_3469delinsAG	XP_006717953.1:p.Glu1156=
XM_011539849.1:c.4392_4393delinsAG	XP_011538151.1:p.Glu1464=
XM_011539850.1:c.3237_3238delinsAG	XP_011538152.1:p.Glu1079=
XM_011539851.1:c.4392_4393delinsAG	XP_011538153.1:p.Glu1464=
XM_011539852.1:c.4392_4393delinsAG	XP_011538154.1:p.Glu1464=
XM_006717885.4:c.4392_4393delinsAG	XP_006717948.1:p.Glu1464=
XM_006717888.4:c.4392_4393delinsAG	XP_006717951.1:p.Glu1464=
XM_006717889.4:c.4344_4345delinsAG	XP_006717952.1:p.Glu1448=
XM_006717890.3:c.3468_3469delinsAG	XP_006717953.1:p.Glu1156=
XM_011539849.3:c.4392_4393delinsAG	XP_011538151.1:p.Glu1464=
XM_011539850.3:c.3237_3238delinsAG	XP_011538152.1:p.Glu1079=
XM_011539851.3:c.4392_4393delinsAG	XP_011538153.1:p.Glu1464=
XM_011539852.3:c.4392_4393delinsAG	XP_011538154.1:p.Glu1464=
XM_017016310.2:c.4392_4393delinsAG	XP_016871799.1:p.Glu1464=
XM_017016311.2:c.4392_4393delinsAG	XP_016871800.1:p.Glu1464=
XM_017016312.2:c.3420_3421delinsAG	XP_016871801.1:p.Glu1140=
NM_001288989.2:c.4344_4345delinsAG	NP_001275918.1:p.Glu1448=
NM_016341.4:c.4392_4393delinsAG MANE Select	NP_057425.3:p.Glu1464=