Canonical Allele Identifier: CA1183549148
Gene: PLPPR5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.98987730_98987732delinsATG , CM000663.2:g.98987730_98987732delinsATG GRCh38
NC_000001.10:g.99453286_99453288delinsATG , CM000663.1:g.99453286_99453288delinsATG GRCh37
NC_000001.9:g.99225874_99225876delinsATG NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000696571.1:c.73-30991_73-30989delinsCAT ENSP00000512726.1:n.73-30991_73-30989delinsCAT
ENST00000263177.5:c.237+16703_237+16705delinsCAT MANE Select ENSP00000263177.4:n.237+16703_237+16705delinsCAT
ENST00000672681.1:c.237+16703_237+16705delinsCAT ENSP00000500930.1:n.237+16703_237+16705delinsCAT
ENST00000263177.4:c.237+16703_237+16705delinsCAT ENSP00000263177.4:n.237+16703_237+16705delinsCAT
ENST00000370188.7:c.237+16703_237+16705delinsCAT ENSP00000359207.3:n.237+16703_237+16705delinsCAT
NM_001010861.2:c.237+16703_237+16705delinsCAT NP_001010861.1:n.237+16703_237+16705delinsCAT
NM_001037317.1:c.237+16703_237+16705delinsCAT NP_001032394.1:n.237+16703_237+16705delinsCAT
XM_011540836.1:c.237+16703_237+16705delinsCAT XP_011539138.1:n.237+16703_237+16705delinsCAT
XM_011540837.1:c.237+16703_237+16705delinsCAT XP_011539139.1:n.237+16703_237+16705delinsCAT
XM_011540838.1:c.189+16703_189+16705delinsCAT XP_011539140.1:n.189+16703_189+16705delinsCAT
XM_011540839.1:c.189+16703_189+16705delinsCAT XP_011539141.1:n.189+16703_189+16705delinsCAT
XM_011540836.2:c.237+16703_237+16705delinsCAT XP_011539138.1:n.237+16703_237+16705delinsCAT
XM_011540838.3:c.189+16703_189+16705delinsCAT XP_011539140.1:n.189+16703_189+16705delinsCAT
NM_001037317.2:c.237+16703_237+16705delinsCAT MANE Select NP_001032394.1:n.237+16703_237+16705delinsCAT
NM_001010861.3:c.237+16703_237+16705delinsCAT NP_001010861.1:n.237+16703_237+16705delinsCAT