Canonical Allele Identifier: CA1928996210

Gene: PLCE1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94293623_94293624delinsCA , CM000672.2:g.94293623_94293624delinsCA	GRCh38
NC_000010.10:g.96053380_96053381delinsCA , CM000672.1:g.96053380_96053381delinsCA	GRCh37
NC_000010.9:g.96043370_96043371delinsCA	NCBI36
NG_015799.1:g.304635_304636delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.4227_4228delinsCA	ENSP00000360426.1:p.Asn1409=
ENST00000685253.1:c.*1694_*1695delinsCA	ENSP00000509405.1:n.*1694_*1695delinsCA
ENST00000685889.1:n.1886_1887delinsCA
ENST00000686807.1:n.570_571delinsCA
ENST00000686954.1:c.*435_*436delinsCA	ENSP00000508416.1:n.*435_*436delinsCA
ENST00000688810.1:c.4179_4180delinsCA	ENSP00000509140.1:p.Asn1393=
ENST00000689233.1:n.9359_9360delinsCA
ENST00000690340.1:n.2824_2825delinsCA
ENST00000692286.1:c.5036-4756_5036-4755delinsCA	ENSP00000509490.1:n.5036-4756_5036-4755delinsCA
ENST00000692396.1:c.5103_5104delinsCA	ENSP00000508605.1:p.Asn1701=
ENST00000371380.8:c.5151_5152delinsCA MANE Select	ENSP00000360431.2:p.Asn1717=
ENST00000371385.8:c.4125_4126delinsCA	ENSP00000360438.4:p.Asn1375=
ENST00000674738.1:c.3706_3707delinsCA
ENST00000674827.1:c.3267_3268delinsCA	ENSP00000502523.1:p.Asn1089=
ENST00000675218.1:c.4227_4228delinsCA	ENSP00000501910.1:p.Asn1409=
ENST00000675487.1:c.*1084_*1085delinsCA	ENSP00000502340.1:n.*1084_*1085delinsCA
ENST00000675718.1:c.4420_4421delinsCA
ENST00000676102.1:c.3996_3997delinsCA	ENSP00000502811.1:p.Asn1332=
ENST00000260766.7:c.5151_5152delinsCA	ENSP00000260766.3:p.Asn1717=
ENST00000371375.1:c.4227_4228delinsCA	ENSP00000360426.1:p.Asn1409=
ENST00000371380.7:c.5151_5152delinsCA	ENSP00000360431.2:p.Asn1717=
ENST00000371385.7:c.4227_4228delinsCA	ENSP00000360438.3:p.Asn1409=
NM_001165979.2:c.4227_4228delinsCA	NP_001159451.1:p.Asn1409=
NM_001288989.1:c.5103_5104delinsCA	NP_001275918.1:p.Asn1701=
NM_016341.3:c.5151_5152delinsCA	NP_057425.3:p.Asn1717=
XM_006717885.2:c.5193_5194delinsCA	XP_006717948.1:p.Asn1731=
XM_006717886.2:c.5193_5194delinsCA	XP_006717949.1:p.Asn1731=
XM_006717888.2:c.5190_5191delinsCA	XP_006717951.1:p.Asn1730=
XM_006717889.2:c.5145_5146delinsCA	XP_006717952.1:p.Asn1715=
XM_006717890.1:c.4269_4270delinsCA	XP_006717953.1:p.Asn1423=
XM_011539849.1:c.5193_5194delinsCA	XP_011538151.1:p.Asn1731=
XM_011539850.1:c.4038_4039delinsCA	XP_011538152.1:p.Asn1346=
XM_006717885.4:c.5193_5194delinsCA	XP_006717948.1:p.Asn1731=
XM_006717888.4:c.5190_5191delinsCA	XP_006717951.1:p.Asn1730=
XM_006717889.4:c.5145_5146delinsCA	XP_006717952.1:p.Asn1715=
XM_006717890.3:c.4269_4270delinsCA	XP_006717953.1:p.Asn1423=
XM_011539849.3:c.5193_5194delinsCA	XP_011538151.1:p.Asn1731=
XM_011539850.3:c.4038_4039delinsCA	XP_011538152.1:p.Asn1346=
XM_017016310.2:c.5193_5194delinsCA	XP_016871799.1:p.Asn1731=
XM_017016311.2:c.5193_5194delinsCA	XP_016871800.1:p.Asn1731=
XM_017016312.2:c.4179_4180delinsCA	XP_016871801.1:p.Asn1393=
NM_001288989.2:c.5103_5104delinsCA	NP_001275918.1:p.Asn1701=
NM_016341.4:c.5151_5152delinsCA MANE Select	NP_057425.3:p.Asn1717=