Canonical Allele Identifier: CA2203529386

Gene: ROGDI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4798416G= , CM000678.2:g.4798416G=	GRCh38
NC_000016.9:g.4848417G= , CM000678.1:g.4848417G=	GRCh37
NC_000016.8:g.4788418G=	NCBI36
NG_032174.1:g.9535C= , LRG_455:g.9535C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.531+153C= MANE Select	ENSP00000322832.6:n.531+153C=
ENST00000322048.11:c.531+153C=	ENSP00000322832.5:n.531+153C=
ENST00000586153.1:c.178-232C=	ENSP00000464699.1:n.178-232C=
ENST00000586336.5:n.630+153C=
ENST00000586504.5:c.311+153C=
ENST00000587377.5:c.544+153C=	ENSP00000468343.1:n.544+153C=
ENST00000587711.5:c.216+153C=	ENSP00000467459.1:n.216+153C=
ENST00000587843.5:c.*269+153C=	ENSP00000465970.1:n.*269+153C=
ENST00000588201.5:c.*522+153C=	ENSP00000466529.1:n.*522+153C=
ENST00000589543.5:n.488+153C=
ENST00000591292.5:n.1860+153C=
ENST00000591392.5:c.459+153C=	ENSP00000467509.1:n.459+153C=
ENST00000592019.1:c.77-601C=
NM_024589.2:c.531+153C= , LRG_455t1:c.531+153C=	NP_078865.1:n.531+153C=
NR_046480.1:n.855+153C=
XM_006720947.2:c.531+153C=	XP_006721010.1:n.531+153C=
XM_006720948.2:c.261+153C=	XP_006721011.1:n.261+153C=
XM_006720947.4:c.531+153C=	XP_006721010.1:n.531+153C=
XM_006720948.4:c.261+153C=	XP_006721011.1:n.261+153C=
NM_024589.3:c.531+153C= MANE Select	NP_078865.1:n.531+153C=
NR_046480.2:n.538+153C=