Canonical Allele Identifier: CA2203529215

Gene: ROGDI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4798169C= , CM000678.2:g.4798169C=	GRCh38
NC_000016.9:g.4848170C= , CM000678.1:g.4848170C=	GRCh37
NC_000016.8:g.4788171C=	NCBI36
NG_032174.1:g.9782G= , LRG_455:g.9782G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.547G= MANE Select	ENSP00000322832.6:p.Ala183=
ENST00000322048.11:c.547G=	ENSP00000322832.5:p.Ala183=
ENST00000586153.1:c.193G=	ENSP00000464699.1:p.Ala65=
ENST00000586336.5:n.646G=
ENST00000586504.5:c.327G=
ENST00000587377.5:c.560G=	ENSP00000468343.1:p.Cys187=
ENST00000587711.5:c.232G=	ENSP00000467459.1:p.Ala78=
ENST00000587843.5:c.*285G=	ENSP00000465970.1:n.*285G=
ENST00000588201.5:c.*538G=	ENSP00000466529.1:n.*538G=
ENST00000589543.5:n.504G=
ENST00000591292.5:n.1876G=
ENST00000591392.5:c.475G=	ENSP00000467509.1:p.Ala159=
ENST00000592019.1:c.77-354G=
NM_024589.2:c.547G= , LRG_455t1:c.547G=	NP_078865.1:p.Ala183=
NR_046480.1:n.871G=
XM_006720947.2:c.547G=	XP_006721010.1:p.Ala183=
XM_006720948.2:c.277G=	XP_006721011.1:p.Ala93=
XM_006720947.4:c.547G=	XP_006721010.1:p.Ala183=
XM_006720948.4:c.277G=	XP_006721011.1:p.Ala93=
NM_024589.3:c.547G= MANE Select	NP_078865.1:p.Ala183=
NR_046480.2:n.554G=