Canonical Allele Identifier: CA2805667692
Gene: ROGDI HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.4797921_4797922insCAAAC , CM000678.2:g.4797921_4797922insCAAAC GRCh38
NC_000016.9:g.4847922_4847923insCAAAC , CM000678.1:g.4847922_4847923insCAAAC GRCh37
NC_000016.8:g.4787923_4787924insCAAAC NCBI36
NG_032174.1:g.10030_10031insTTTGG , LRG_455:g.10030_10031insTTTGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000322048.12:c.695+17_695+18insTTTGG MANE Select ENSP00000322832.6:n.695+17_695+18insTTTGG
ENST00000322048.11:c.695+17_695+18insTTTGG ENSP00000322832.5:n.695+17_695+18insTTTGG
ENST00000586153.1:c.341+17_341+18insTTTGG ENSP00000464699.1:n.341+17_341+18insTTTGG
ENST00000586336.5:n.794+17_794+18insTTTGG
ENST00000586504.5:c.426-81_426-80insTTTGG
ENST00000587377.5:c.*15+17_*15+18insTTTGG ENSP00000468343.1:n.*15+17_*15+18insTTTGG
ENST00000587711.5:c.380+17_380+18insTTTGG ENSP00000467459.1:n.380+17_380+18insTTTGG
ENST00000587843.5:c.*433+17_*433+18insTTTGG ENSP00000465970.1:n.*433+17_*433+18insTTTGG
ENST00000588201.5:c.*686+17_*686+18insTTTGG ENSP00000466529.1:n.*686+17_*686+18insTTTGG
ENST00000589543.5:n.652+17_652+18insTTTGG
ENST00000591292.5:n.2024+17_2024+18insTTTGG
ENST00000591392.5:c.623+17_623+18insTTTGG ENSP00000467509.1:n.623+17_623+18insTTTGG
ENST00000592019.1:c.77-106_77-105insTTTGG
NM_024589.2:c.695+17_695+18insTTTGG , LRG_455t1:c.695+17_695+18insTTTGG NP_078865.1:n.695+17_695+18insTTTGG
NR_046480.1:n.1019+17_1019+18insTTTGG
XM_006720947.2:c.695+17_695+18insTTTGG XP_006721010.1:n.695+17_695+18insTTTGG
XM_006720948.2:c.425+17_425+18insTTTGG XP_006721011.1:n.425+17_425+18insTTTGG
XM_006720947.4:c.695+17_695+18insTTTGG XP_006721010.1:n.695+17_695+18insTTTGG
XM_006720948.4:c.425+17_425+18insTTTGG XP_006721011.1:n.425+17_425+18insTTTGG
NM_024589.3:c.695+17_695+18insTTTGG MANE Select NP_078865.1:n.695+17_695+18insTTTGG
NR_046480.2:n.702+17_702+18insTTTGG