Canonical Allele Identifier: CA1928998336
Gene: PLCE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94298326_94298348delinsAAATATTTAAAGTTTTCTACACT , CM000672.2:g.94298326_94298348delinsAAATATTTAAAGTTTTCTACACT GRCh38
NC_000010.10:g.96058083_96058105delinsAAATATTTAAAGTTTTCTACACT , CM000672.1:g.96058083_96058105delinsAAATATTTAAAGTTTTCTACACT GRCh37
NC_000010.9:g.96048073_96048095delinsAAATATTTAAAGTTTTCTACACT NCBI36
NG_015799.1:g.309338_309360delinsAAATATTTAAAGTTTTCTACACT

Transcript Alleles

HGVS Amino-acid change
ENST00000371380.8:c.5168-53_5168-31delinsAAATATTTAAAGTTTTCTACACT MANE Select ENSP00000360431.2:p.=
ENST00000371385.8:c.4142-53_4142-31delinsAAATATTTAAAGTTTTCTACACT ENSP00000360438.4:p.=
ENST00000674738.1:n.3723-53_3723-31delinsAAATATTTAAAGTTTTCTACACT
ENST00000674827.1:n.3284-53_3284-31delinsAAATATTTAAAGTTTTCTACACT ENSP00000502523.1:p.=
ENST00000675218.1:n.4244-53_4244-31delinsAAATATTTAAAGTTTTCTACACT ENSP00000501910.1:p.=
ENST00000675487.1:c.*1101-53_*1101-31delinsAAATATTTAAAGTTTTCTACACT ENSP00000502340.1:p.=
ENST00000675718.1:n.4437-53_4437-31delinsAAATATTTAAAGTTTTCTACACT
ENST00000676102.1:c.4013-53_4013-31delinsAAATATTTAAAGTTTTCTACACT ENSP00000502811.1:p.=
ENST00000260766.7:c.5168-53_5168-31delinsAAATATTTAAAGTTTTCTACACT ENSP00000260766.3:p.=
ENST00000371375.1:n.4244-53_4244-31delinsAAATATTTAAAGTTTTCTACACT ENSP00000360426.1:p.=
ENST00000371380.7:c.5168-53_5168-31delinsAAATATTTAAAGTTTTCTACACT ENSP00000360431.2:p.=
ENST00000371385.7:c.4244-53_4244-31delinsAAATATTTAAAGTTTTCTACACT ENSP00000360438.3:p.=
NM_001165979.2:c.4244-53_4244-31delinsAAATATTTAAAGTTTTCTACACT NP_001159451.1:p.=
NM_001288989.1:c.5120-53_5120-31delinsAAATATTTAAAGTTTTCTACACT NP_001275918.1:p.=
NM_016341.3:c.5168-53_5168-31delinsAAATATTTAAAGTTTTCTACACT NP_057425.3:p.=
XM_006717885.2:c.5210-53_5210-31delinsAAATATTTAAAGTTTTCTACACT XP_006717948.1:p.=
XM_006717886.2:c.5210-53_5210-31delinsAAATATTTAAAGTTTTCTACACT XP_006717949.1:p.=
XM_006717888.2:c.5207-53_5207-31delinsAAATATTTAAAGTTTTCTACACT XP_006717951.1:p.=
XM_006717889.2:c.5162-53_5162-31delinsAAATATTTAAAGTTTTCTACACT XP_006717952.1:p.=
XM_006717890.1:c.4286-53_4286-31delinsAAATATTTAAAGTTTTCTACACT XP_006717953.1:p.=
XM_011539849.1:c.5210-53_5210-31delinsAAATATTTAAAGTTTTCTACACT XP_011538151.1:p.=
XM_011539850.1:c.4055-53_4055-31delinsAAATATTTAAAGTTTTCTACACT XP_011538152.1:p.=
XM_006717885.4:c.5210-53_5210-31delinsAAATATTTAAAGTTTTCTACACT XP_006717948.1:p.=
XM_006717888.4:c.5207-53_5207-31delinsAAATATTTAAAGTTTTCTACACT XP_006717951.1:p.=
XM_006717889.4:c.5162-53_5162-31delinsAAATATTTAAAGTTTTCTACACT XP_006717952.1:p.=
XM_006717890.3:c.4286-53_4286-31delinsAAATATTTAAAGTTTTCTACACT XP_006717953.1:p.=
XM_011539849.3:c.5210-53_5210-31delinsAAATATTTAAAGTTTTCTACACT XP_011538151.1:p.=
XM_011539850.3:c.4055-53_4055-31delinsAAATATTTAAAGTTTTCTACACT XP_011538152.1:p.=
XM_017016310.2:c.5210-53_5210-31delinsAAATATTTAAAGTTTTCTACACT XP_016871799.1:p.=
XM_017016311.2:c.5210-53_5210-31delinsAAATATTTAAAGTTTTCTACACT XP_016871800.1:p.=
XM_017016312.2:c.4196-53_4196-31delinsAAATATTTAAAGTTTTCTACACT XP_016871801.1:p.=
NM_001288989.2:c.5120-53_5120-31delinsAAATATTTAAAGTTTTCTACACT NP_001275918.1:p.=
NM_016341.4:c.5168-53_5168-31delinsAAATATTTAAAGTTTTCTACACT MANE Select NP_057425.3:p.=