Canonical Allele Identifier: CA2203529067

Gene: ROGDI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4797981G= , CM000678.2:g.4797981G=	GRCh38
NC_000016.9:g.4847982G= , CM000678.1:g.4847982G=	GRCh37
NC_000016.8:g.4787983G=	NCBI36
NG_032174.1:g.9970C= , LRG_455:g.9970C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.652C= MANE Select	ENSP00000322832.6:p.Arg218=
ENST00000322048.11:c.652C=	ENSP00000322832.5:p.Arg218=
ENST00000586153.1:c.298C=	ENSP00000464699.1:p.Arg100=
ENST00000586336.5:n.751C=
ENST00000586504.5:c.425+90C=
ENST00000587377.5:c.665C=	ENSP00000468343.1:p.Pro222=
ENST00000587711.5:c.337C=	ENSP00000467459.1:p.Arg113=
ENST00000587843.5:c.*390C=	ENSP00000465970.1:n.*390C=
ENST00000588201.5:c.*643C=	ENSP00000466529.1:n.*643C=
ENST00000589543.5:n.609C=
ENST00000591292.5:n.1981C=
ENST00000591392.5:c.580C=	ENSP00000467509.1:p.Arg194=
ENST00000592019.1:c.77-166C=
NM_024589.2:c.652C= , LRG_455t1:c.652C=	NP_078865.1:p.Arg218=
NR_046480.1:n.976C=
XM_006720947.2:c.652C=	XP_006721010.1:p.Arg218=
XM_006720948.2:c.382C=	XP_006721011.1:p.Arg128=
XM_006720947.4:c.652C=	XP_006721010.1:p.Arg218=
XM_006720948.4:c.382C=	XP_006721011.1:p.Arg128=
NM_024589.3:c.652C= MANE Select	NP_078865.1:p.Arg218=
NR_046480.2:n.659C=