Canonical Allele Identifier: CA2203529065

Gene: ROGDI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4797979G= , CM000678.2:g.4797979G=	GRCh38
NC_000016.9:g.4847980G= , CM000678.1:g.4847980G=	GRCh37
NC_000016.8:g.4787981G=	NCBI36
NG_032174.1:g.9972C= , LRG_455:g.9972C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.654C= MANE Select	ENSP00000322832.6:p.Arg218=
ENST00000322048.11:c.654C=	ENSP00000322832.5:p.Arg218=
ENST00000586153.1:c.300C=	ENSP00000464699.1:p.Arg100=
ENST00000586336.5:n.753C=
ENST00000586504.5:c.425+92C=
ENST00000587377.5:c.667C=	ENSP00000468343.1:p.Pro223=
ENST00000587711.5:c.339C=	ENSP00000467459.1:p.Arg113=
ENST00000587843.5:c.*392C=	ENSP00000465970.1:n.*392C=
ENST00000588201.5:c.*645C=	ENSP00000466529.1:n.*645C=
ENST00000589543.5:n.611C=
ENST00000591292.5:n.1983C=
ENST00000591392.5:c.582C=	ENSP00000467509.1:p.Arg194=
ENST00000592019.1:c.77-164C=
NM_024589.2:c.654C= , LRG_455t1:c.654C=	NP_078865.1:p.Arg218=
NR_046480.1:n.978C=
XM_006720947.2:c.654C=	XP_006721010.1:p.Arg218=
XM_006720948.2:c.384C=	XP_006721011.1:p.Arg128=
XM_006720947.4:c.654C=	XP_006721010.1:p.Arg218=
XM_006720948.4:c.384C=	XP_006721011.1:p.Arg128=
NM_024589.3:c.654C= MANE Select	NP_078865.1:p.Arg218=
NR_046480.2:n.661C=