Canonical Allele Identifier: CA2631551567
Gene: ROGDI HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.4798444_4798445insT , CM000678.2:g.4798444_4798445insT GRCh38
NC_000016.9:g.4848445_4848446insT , CM000678.1:g.4848445_4848446insT GRCh37
NC_000016.8:g.4788446_4788447insT NCBI36
NG_032174.1:g.9506_9507insA , LRG_455:g.9506_9507insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000322048.12:c.531+124_531+125insA MANE Select ENSP00000322832.6:n.531+124_531+125insA
ENST00000322048.11:c.531+124_531+125insA ENSP00000322832.5:n.531+124_531+125insA
ENST00000586153.1:c.178-261_178-260insA ENSP00000464699.1:n.178-261_178-260insA
ENST00000586336.5:n.630+124_630+125insA
ENST00000586504.5:c.311+124_311+125insA
ENST00000587377.5:c.544+124_544+125insA ENSP00000468343.1:n.544+124_544+125insA
ENST00000587711.5:c.216+124_216+125insA ENSP00000467459.1:n.216+124_216+125insA
ENST00000587843.5:c.*269+124_*269+125insA ENSP00000465970.1:n.*269+124_*269+125insA
ENST00000588201.5:c.*522+124_*522+125insA ENSP00000466529.1:n.*522+124_*522+125insA
ENST00000589543.5:n.488+124_488+125insA
ENST00000591292.5:n.1860+124_1860+125insA
ENST00000591392.5:c.459+124_459+125insA ENSP00000467509.1:n.459+124_459+125insA
ENST00000592019.1:c.77-630_77-629insA
NM_024589.2:c.531+124_531+125insA , LRG_455t1:c.531+124_531+125insA NP_078865.1:n.531+124_531+125insA
NR_046480.1:n.855+124_855+125insA
XM_006720947.2:c.531+124_531+125insA XP_006721010.1:n.531+124_531+125insA
XM_006720948.2:c.261+124_261+125insA XP_006721011.1:n.261+124_261+125insA
XM_006720947.4:c.531+124_531+125insA XP_006721010.1:n.531+124_531+125insA
XM_006720948.4:c.261+124_261+125insA XP_006721011.1:n.261+124_261+125insA
NM_024589.3:c.531+124_531+125insA MANE Select NP_078865.1:n.531+124_531+125insA
NR_046480.2:n.538+124_538+125insA