Canonical Allele Identifier: CA2631551460
Gene: ROGDI HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.4798406_4798435del , CM000678.2:g.4798406_4798435del GRCh38
NC_000016.9:g.4848407_4848436del , CM000678.1:g.4848407_4848436del GRCh37
NC_000016.8:g.4788408_4788437del NCBI36
NG_032174.1:g.9516_9545del , LRG_455:g.9516_9545del

Transcript Alleles

HGVS Amino-acid Change
ENST00000322048.12:c.531+134_531+163del MANE Select ENSP00000322832.6:n.531+134_531+163del
ENST00000322048.11:c.531+134_531+163del ENSP00000322832.5:n.531+134_531+163del
ENST00000586153.1:c.178-251_178-222del ENSP00000464699.1:n.178-251_178-222del
ENST00000586336.5:n.630+134_630+163del
ENST00000586504.5:c.311+134_311+163del
ENST00000587377.5:c.544+134_544+163del ENSP00000468343.1:n.544+134_544+163del
ENST00000587711.5:c.216+134_216+163del ENSP00000467459.1:n.216+134_216+163del
ENST00000587843.5:c.*269+134_*269+163del ENSP00000465970.1:n.*269+134_*269+163del
ENST00000588201.5:c.*522+134_*522+163del ENSP00000466529.1:n.*522+134_*522+163del
ENST00000589543.5:n.488+134_488+163del
ENST00000591292.5:n.1860+134_1860+163del
ENST00000591392.5:c.459+134_459+163del ENSP00000467509.1:n.459+134_459+163del
ENST00000592019.1:c.77-620_77-591del
NM_024589.2:c.531+134_531+163del , LRG_455t1:c.531+134_531+163del NP_078865.1:n.531+134_531+163del
NR_046480.1:n.855+134_855+163del
XM_006720947.2:c.531+134_531+163del XP_006721010.1:n.531+134_531+163del
XM_006720948.2:c.261+134_261+163del XP_006721011.1:n.261+134_261+163del
XM_006720947.4:c.531+134_531+163del XP_006721010.1:n.531+134_531+163del
XM_006720948.4:c.261+134_261+163del XP_006721011.1:n.261+134_261+163del
NM_024589.3:c.531+134_531+163del MANE Select NP_078865.1:n.531+134_531+163del
NR_046480.2:n.538+134_538+163del