Canonical Allele Identifier: CA2203529379

Gene: ROGDI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4798408G= , CM000678.2:g.4798408G=	GRCh38
NC_000016.9:g.4848409G= , CM000678.1:g.4848409G=	GRCh37
NC_000016.8:g.4788410G=	NCBI36
NG_032174.1:g.9543C= , LRG_455:g.9543C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.531+161C= MANE Select	ENSP00000322832.6:n.531+161C=
ENST00000322048.11:c.531+161C=	ENSP00000322832.5:n.531+161C=
ENST00000586153.1:c.178-224C=	ENSP00000464699.1:n.178-224C=
ENST00000586336.5:n.630+161C=
ENST00000586504.5:c.311+161C=
ENST00000587377.5:c.544+161C=	ENSP00000468343.1:n.544+161C=
ENST00000587711.5:c.216+161C=	ENSP00000467459.1:n.216+161C=
ENST00000587843.5:c.*269+161C=	ENSP00000465970.1:n.*269+161C=
ENST00000588201.5:c.*522+161C=	ENSP00000466529.1:n.*522+161C=
ENST00000589543.5:n.488+161C=
ENST00000591292.5:n.1860+161C=
ENST00000591392.5:c.459+161C=	ENSP00000467509.1:n.459+161C=
ENST00000592019.1:c.77-593C=
NM_024589.2:c.531+161C= , LRG_455t1:c.531+161C=	NP_078865.1:n.531+161C=
NR_046480.1:n.855+161C=
XM_006720947.2:c.531+161C=	XP_006721010.1:n.531+161C=
XM_006720948.2:c.261+161C=	XP_006721011.1:n.261+161C=
XM_006720947.4:c.531+161C=	XP_006721010.1:n.531+161C=
XM_006720948.4:c.261+161C=	XP_006721011.1:n.261+161C=
NM_024589.3:c.531+161C= MANE Select	NP_078865.1:n.531+161C=
NR_046480.2:n.538+161C=