Canonical Allele Identifier: CA2731571421

Gene: ROGDI

Linked Data

• dbSNP Id: rs372237238

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4798028G>C , CM000678.2:g.4798028G>C	GRCh38
NC_000016.9:g.4848029G>C , CM000678.1:g.4848029G>C	GRCh37
NC_000016.8:g.4788030G>C	NCBI36
NG_032174.1:g.9923C>G , LRG_455:g.9923C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.646-41C>G MANE Select	ENSP00000322832.6:n.646-41C>G
ENST00000322048.11:c.646-41C>G	ENSP00000322832.5:n.646-41C>G
ENST00000586153.1:c.292-41C>G	ENSP00000464699.1:n.292-41C>G
ENST00000586336.5:n.745-41C>G
ENST00000586504.5:c.425+43C>G
ENST00000587377.5:c.659-41C>G	ENSP00000468343.1:n.659-41C>G
ENST00000587711.5:c.331-41C>G	ENSP00000467459.1:n.331-41C>G
ENST00000587843.5:c.*384-41C>G	ENSP00000465970.1:n.*384-41C>G
ENST00000588201.5:c.*637-41C>G	ENSP00000466529.1:n.*637-41C>G
ENST00000589543.5:n.603-41C>G
ENST00000591292.5:n.1975-41C>G
ENST00000591392.5:c.574-41C>G	ENSP00000467509.1:n.574-41C>G
ENST00000592019.1:c.77-213C>G
NM_024589.2:c.646-41C>G , LRG_455t1:c.646-41C>G	NP_078865.1:n.646-41C>G
NR_046480.1:n.970-41C>G
XM_006720947.2:c.646-41C>G	XP_006721010.1:n.646-41C>G
XM_006720948.2:c.376-41C>G	XP_006721011.1:n.376-41C>G
XM_006720947.4:c.646-41C>G	XP_006721010.1:n.646-41C>G
XM_006720948.4:c.376-41C>G	XP_006721011.1:n.376-41C>G
NM_024589.3:c.646-41C>G MANE Select	NP_078865.1:n.646-41C>G
NR_046480.2:n.653-41C>G