Canonical Allele Identifier: CA2203529068

Gene: ROGDI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4797982G= , CM000678.2:g.4797982G=	GRCh38
NC_000016.9:g.4847983G= , CM000678.1:g.4847983G=	GRCh37
NC_000016.8:g.4787984G=	NCBI36
NG_032174.1:g.9969C= , LRG_455:g.9969C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.651C= MANE Select	ENSP00000322832.6:p.Phe217=
ENST00000322048.11:c.651C=	ENSP00000322832.5:p.Phe217=
ENST00000586153.1:c.297C=	ENSP00000464699.1:p.Phe99=
ENST00000586336.5:n.750C=
ENST00000586504.5:c.425+89C=
ENST00000587377.5:c.664C=	ENSP00000468343.1:p.Pro222=
ENST00000587711.5:c.336C=	ENSP00000467459.1:p.Phe112=
ENST00000587843.5:c.*389C=	ENSP00000465970.1:n.*389C=
ENST00000588201.5:c.*642C=	ENSP00000466529.1:n.*642C=
ENST00000589543.5:n.608C=
ENST00000591292.5:n.1980C=
ENST00000591392.5:c.579C=	ENSP00000467509.1:p.Phe193=
ENST00000592019.1:c.77-167C=
NM_024589.2:c.651C= , LRG_455t1:c.651C=	NP_078865.1:p.Phe217=
NR_046480.1:n.975C=
XM_006720947.2:c.651C=	XP_006721010.1:p.Phe217=
XM_006720948.2:c.381C=	XP_006721011.1:p.Phe127=
XM_006720947.4:c.651C=	XP_006721010.1:p.Phe217=
XM_006720948.4:c.381C=	XP_006721011.1:p.Phe127=
NM_024589.3:c.651C= MANE Select	NP_078865.1:p.Phe217=
NR_046480.2:n.658C=