Canonical Allele Identifier: CA2203528977
Gene: ROGDI HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.4797873_4797907delinsCCCGGCCCTCCAGGTGTGGAGGGATGGGGTGGGCG , CM000678.2:g.4797873_4797907delinsCCCGGCCCTCCAGGTGTGGAGGGATGGGGTGGGCG GRCh38
NC_000016.9:g.4847874_4847908delinsCCCGGCCCTCCAGGTGTGGAGGGATGGGGTGGGCG , CM000678.1:g.4847874_4847908delinsCCCGGCCCTCCAGGTGTGGAGGGATGGGGTGGGCG GRCh37
NC_000016.8:g.4787875_4787909delinsCCCGGCCCTCCAGGTGTGGAGGGATGGGGTGGGCG NCBI36
NG_032174.1:g.10044_10078delinsCGCCCACCCCATCCCTCCACACCTGGAGGGCCGGG , LRG_455:g.10044_10078delinsCGCCCACCCCATCCCTCCACACCTGGAGGGCCGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000322048.12:c.695+31_696-33delinsCGCCCACCCCATCCCTCCACACCTGGAGGGCCGGG MANE Select ENSP00000322832.6:n.695+31_696-33delinsCGCCCACCCCATCCCTCCACAC...
ENST00000322048.11:c.695+31_696-33delinsCGCCCACCCCATCCCTCCACACCTGGAGGGCCGGG ENSP00000322832.5:n.695+31_696-33delinsCGCCCACCCCATCCCTCCACAC...
ENST00000586153.1:c.341+31_342-37delinsCGCCCACCCCATCCCTCCACACCTGGAGGGCCGGG ENSP00000464699.1:n.341+31_342-37delinsCGCCCACCCCATCCCTCCACAC...
ENST00000586336.5:n.794+31_795-33delinsCGCCCACCCCATCCCTCCACACCTGGAGGGCCGGG
ENST00000586504.5:c.426-67_426-33delinsCGCCCACCCCATCCCTCCACACCTGGAGGGCCGGG
ENST00000587377.5:c.*15+31_*16-33delinsCGCCCACCCCATCCCTCCACACCTGGAGGGCCGGG ENSP00000468343.1:n.*15+31_*16-33delinsCGCCCACCCCATCCCTCCACAC...
ENST00000587711.5:c.380+31_381-33delinsCGCCCACCCCATCCCTCCACACCTGGAGGGCCGGG ENSP00000467459.1:n.380+31_381-33delinsCGCCCACCCCATCCCTCCACAC...
ENST00000587843.5:c.*433+31_*434-33delinsCGCCCACCCCATCCCTCCACACCTGGAGGGCCGGG ENSP00000465970.1:n.*433+31_*434-33delinsCGCCCACCCCATCCCTCCAC...
ENST00000588201.5:c.*686+31_*687-33delinsCGCCCACCCCATCCCTCCACACCTGGAGGGCCGGG ENSP00000466529.1:n.*686+31_*687-33delinsCGCCCACCCCATCCCTCCAC...
ENST00000589543.5:n.652+31_653-33delinsCGCCCACCCCATCCCTCCACACCTGGAGGGCCGGG
ENST00000591292.5:n.2024+31_2025-33delinsCGCCCACCCCATCCCTCCACACCTGGAGGGCCGGG
ENST00000591392.5:c.623+31_624-33delinsCGCCCACCCCATCCCTCCACACCTGGAGGGCCGGG ENSP00000467509.1:n.623+31_624-33delinsCGCCCACCCCATCCCTCCACAC...
ENST00000592019.1:c.77-92_77-58delinsCGCCCACCCCATCCCTCCACACCTGGAGGGCCGGG
NM_024589.2:c.695+31_696-33delinsCGCCCACCCCATCCCTCCACACCTGGAGGGCCGGG , LRG_455t1:c.695+31_696-33delinsCGCCCACCCCATCCCTCCACACCTGGAGGGCCGGG NP_078865.1:n.695+31_696-33delinsCGCCCACCCCATCCCTCCACACCTGGAG...
NR_046480.1:n.1019+31_1020-33delinsCGCCCACCCCATCCCTCCACACCTGGAGGGCCGGG
XM_006720947.2:c.695+31_696-12delinsCGCCCACCCCATCCCTCCACACCTGGAGGGCCGGG XP_006721010.1:n.695+31_696-12delinsCGCCCACCCCATCCCTCCACACCTG...
XM_006720948.2:c.425+31_426-12delinsCGCCCACCCCATCCCTCCACACCTGGAGGGCCGGG XP_006721011.1:n.425+31_426-12delinsCGCCCACCCCATCCCTCCACACCTG...
XM_006720947.4:c.695+31_696-12delinsCGCCCACCCCATCCCTCCACACCTGGAGGGCCGGG XP_006721010.1:n.695+31_696-12delinsCGCCCACCCCATCCCTCCACACCTG...
XM_006720948.4:c.425+31_426-12delinsCGCCCACCCCATCCCTCCACACCTGGAGGGCCGGG XP_006721011.1:n.425+31_426-12delinsCGCCCACCCCATCCCTCCACACCTG...
NM_024589.3:c.695+31_696-33delinsCGCCCACCCCATCCCTCCACACCTGGAGGGCCGGG MANE Select NP_078865.1:n.695+31_696-33delinsCGCCCACCCCATCCCTCCACACCTGGAG...
NR_046480.2:n.702+31_703-33delinsCGCCCACCCCATCCCTCCACACCTGGAGGGCCGGG