Canonical Allele Identifier: CA2203529218

Gene: ROGDI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4798173G= , CM000678.2:g.4798173G=	GRCh38
NC_000016.9:g.4848174G= , CM000678.1:g.4848174G=	GRCh37
NC_000016.8:g.4788175G=	NCBI36
NG_032174.1:g.9778C= , LRG_455:g.9778C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.543C= MANE Select	ENSP00000322832.6:p.Ala181=
ENST00000322048.11:c.543C=	ENSP00000322832.5:p.Ala181=
ENST00000586153.1:c.189C=	ENSP00000464699.1:p.Ala63=
ENST00000586336.5:n.642C=
ENST00000586504.5:c.323C=
ENST00000587377.5:c.556C=	ENSP00000468343.1:p.Pro186=
ENST00000587711.5:c.228C=	ENSP00000467459.1:p.Ala76=
ENST00000587843.5:c.*281C=	ENSP00000465970.1:n.*281C=
ENST00000588201.5:c.*534C=	ENSP00000466529.1:n.*534C=
ENST00000589543.5:n.500C=
ENST00000591292.5:n.1872C=
ENST00000591392.5:c.471C=	ENSP00000467509.1:p.Ala157=
ENST00000592019.1:c.77-358C=
NM_024589.2:c.543C= , LRG_455t1:c.543C=	NP_078865.1:p.Ala181=
NR_046480.1:n.867C=
XM_006720947.2:c.543C=	XP_006721010.1:p.Ala181=
XM_006720948.2:c.273C=	XP_006721011.1:p.Ala91=
XM_006720947.4:c.543C=	XP_006721010.1:p.Ala181=
XM_006720948.4:c.273C=	XP_006721011.1:p.Ala91=
NM_024589.3:c.543C= MANE Select	NP_078865.1:p.Ala181=
NR_046480.2:n.550C=