Canonical Allele Identifier: CA2843413917
Gene: ROGDI HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.4799794dup , CM000678.2:g.4799794dup GRCh38
NC_000016.9:g.4849795dup , CM000678.1:g.4849795dup GRCh37
NC_000016.8:g.4789796dup NCBI36
NG_032174.1:g.8160dup , LRG_455:g.8160dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000322048.12:c.337-10dup MANE Select ENSP00000322832.6:n.337-10dup
ENST00000322048.11:c.337-10dup ENSP00000322832.5:n.337-10dup
ENST00000585653.1:n.469-10dup
ENST00000586153.1:c.82-10dup ENSP00000464699.1:n.82-10dup
ENST00000586336.5:n.436-10dup
ENST00000586504.5:c.117-10dup
ENST00000587377.5:c.337-10dup ENSP00000468343.1:n.337-10dup
ENST00000587711.5:c.118-1124dup ENSP00000467459.1:n.118-1124dup
ENST00000587843.5:c.*75-10dup ENSP00000465970.1:n.*75-10dup
ENST00000588201.5:c.*194-10dup ENSP00000466529.1:n.*194-10dup
ENST00000589543.5:n.294-10dup
ENST00000591292.5:n.1666-10dup
ENST00000591392.5:c.265-10dup ENSP00000467509.1:n.265-10dup
ENST00000592019.1:c.56-10dup
NM_024589.2:c.337-10dup , LRG_455t1:c.337-10dup NP_078865.1:n.337-10dup
NR_046480.1:n.661-10dup
XM_006720947.2:c.337-10dup XP_006721010.1:n.337-10dup
XM_006720948.2:c.67-10dup XP_006721011.1:n.67-10dup
XM_006720947.4:c.337-10dup XP_006721010.1:n.337-10dup
XM_006720948.4:c.67-10dup XP_006721011.1:n.67-10dup
NM_024589.3:c.337-10dup MANE Select NP_078865.1:n.337-10dup
NR_046480.2:n.344-10dup