Canonical Allele Identifier: CA2203529179

Gene: ROGDI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4798116G= , CM000678.2:g.4798116G=	GRCh38
NC_000016.9:g.4848117G= , CM000678.1:g.4848117G=	GRCh37
NC_000016.8:g.4788118G=	NCBI36
NG_032174.1:g.9835C= , LRG_455:g.9835C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.600C= MANE Select	ENSP00000322832.6:p.Cys200=
ENST00000322048.11:c.600C=	ENSP00000322832.5:p.Cys200=
ENST00000586153.1:c.246C=	ENSP00000464699.1:p.Cys82=
ENST00000586336.5:n.699C=
ENST00000586504.5:c.380C=
ENST00000587377.5:c.613C=	ENSP00000468343.1:p.Pro205=
ENST00000587711.5:c.285C=	ENSP00000467459.1:p.Cys95=
ENST00000587843.5:c.*338C=	ENSP00000465970.1:n.*338C=
ENST00000588201.5:c.*591C=	ENSP00000466529.1:n.*591C=
ENST00000589543.5:n.557C=
ENST00000591292.5:n.1929C=
ENST00000591392.5:c.528C=	ENSP00000467509.1:p.Cys176=
ENST00000592019.1:c.77-301C=
NM_024589.2:c.600C= , LRG_455t1:c.600C=	NP_078865.1:p.Cys200=
NR_046480.1:n.924C=
XM_006720947.2:c.600C=	XP_006721010.1:p.Cys200=
XM_006720948.2:c.330C=	XP_006721011.1:p.Cys110=
XM_006720947.4:c.600C=	XP_006721010.1:p.Cys200=
XM_006720948.4:c.330C=	XP_006721011.1:p.Cys110=
NM_024589.3:c.600C= MANE Select	NP_078865.1:p.Cys200=
NR_046480.2:n.607C=