Canonical Allele Identifier: CA2203530337
Gene: ROGDI HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.4799817C= , CM000678.2:g.4799817C= GRCh38
NC_000016.9:g.4849818C= , CM000678.1:g.4849818C= GRCh37
NC_000016.8:g.4789819C= NCBI36
NG_032174.1:g.8134G= , LRG_455:g.8134G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000322048.12:c.337-36G= MANE Select ENSP00000322832.6:n.337-36G=
ENST00000322048.11:c.337-36G= ENSP00000322832.5:n.337-36G=
ENST00000585653.1:n.469-36G=
ENST00000586153.1:c.82-36G= ENSP00000464699.1:n.82-36G=
ENST00000586336.5:n.436-36G=
ENST00000586504.5:c.117-36G=
ENST00000587377.5:c.337-36G= ENSP00000468343.1:n.337-36G=
ENST00000587711.5:c.118-1150G= ENSP00000467459.1:n.118-1150G=
ENST00000587843.5:c.*75-36G= ENSP00000465970.1:n.*75-36G=
ENST00000588201.5:c.*194-36G= ENSP00000466529.1:n.*194-36G=
ENST00000589543.5:n.294-36G=
ENST00000591292.5:n.1666-36G=
ENST00000591392.5:c.265-36G= ENSP00000467509.1:n.265-36G=
ENST00000592019.1:c.56-36G=
NM_024589.2:c.337-36G= , LRG_455t1:c.337-36G= NP_078865.1:n.337-36G=
NR_046480.1:n.661-36G=
XM_006720947.2:c.337-36G= XP_006721010.1:n.337-36G=
XM_006720948.2:c.67-36G= XP_006721011.1:n.67-36G=
XM_006720947.4:c.337-36G= XP_006721010.1:n.337-36G=
XM_006720948.4:c.67-36G= XP_006721011.1:n.67-36G=
NM_024589.3:c.337-36G= MANE Select NP_078865.1:n.337-36G=
NR_046480.2:n.344-36G=