Canonical Allele Identifier: CA2631550011
Gene: ROGDI HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.4797893_4797909del , CM000678.2:g.4797893_4797909del GRCh38
NC_000016.9:g.4847894_4847910del , CM000678.1:g.4847894_4847910del GRCh37
NC_000016.8:g.4787895_4787911del NCBI36
NG_032174.1:g.10042_10058del , LRG_455:g.10042_10058del

Transcript Alleles

HGVS Amino-acid Change
ENST00000322048.12:c.695+29_695+45del MANE Select ENSP00000322832.6:n.695+29_695+45del
ENST00000322048.11:c.695+29_695+45del ENSP00000322832.5:n.695+29_695+45del
ENST00000586153.1:c.341+29_341+45del ENSP00000464699.1:n.341+29_341+45del
ENST00000586336.5:n.794+29_794+45del
ENST00000586504.5:c.426-69_426-53del
ENST00000587377.5:c.*15+29_*15+45del ENSP00000468343.1:n.*15+29_*15+45del
ENST00000587711.5:c.380+29_380+45del ENSP00000467459.1:n.380+29_380+45del
ENST00000587843.5:c.*433+29_*433+45del ENSP00000465970.1:n.*433+29_*433+45del
ENST00000588201.5:c.*686+29_*686+45del ENSP00000466529.1:n.*686+29_*686+45del
ENST00000589543.5:n.652+29_652+45del
ENST00000591292.5:n.2024+29_2024+45del
ENST00000591392.5:c.623+29_623+45del ENSP00000467509.1:n.623+29_623+45del
ENST00000592019.1:c.77-94_77-78del
NM_024589.2:c.695+29_695+45del , LRG_455t1:c.695+29_695+45del NP_078865.1:n.695+29_695+45del
NR_046480.1:n.1019+29_1019+45del
XM_006720947.2:c.695+29_696-32del XP_006721010.1:n.695+29_696-32del
XM_006720948.2:c.425+29_426-32del XP_006721011.1:n.425+29_426-32del
XM_006720947.4:c.695+29_696-32del XP_006721010.1:n.695+29_696-32del
XM_006720948.4:c.425+29_426-32del XP_006721011.1:n.425+29_426-32del
NM_024589.3:c.695+29_695+45del MANE Select NP_078865.1:n.695+29_695+45del
NR_046480.2:n.702+29_702+45del