Canonical Allele Identifier: CA2203530246

Gene: ROGDI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4799673G= , CM000678.2:g.4799673G=	GRCh38
NC_000016.9:g.4849674G= , CM000678.1:g.4849674G=	GRCh37
NC_000016.8:g.4789675G=	NCBI36
NG_032174.1:g.8278C= , LRG_455:g.8278C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.432+13C= MANE Select	ENSP00000322832.6:n.432+13C=
ENST00000322048.11:c.432+13C=	ENSP00000322832.5:n.432+13C=
ENST00000585653.1:n.564+13C=
ENST00000586153.1:c.177+13C=	ENSP00000464699.1:n.177+13C=
ENST00000586336.5:n.531+13C=
ENST00000586504.5:c.212+13C=
ENST00000587377.5:c.423+22C=	ENSP00000468343.1:n.423+22C=
ENST00000587711.5:c.118-1006C=	ENSP00000467459.1:n.118-1006C=
ENST00000587843.5:c.*170+13C=	ENSP00000465970.1:n.*170+13C=
ENST00000588201.5:c.*289+13C=	ENSP00000466529.1:n.*289+13C=
ENST00000589543.5:n.389+13C=
ENST00000591292.5:n.1761+13C=
ENST00000591392.5:c.360+13C=	ENSP00000467509.1:n.360+13C=
ENST00000592019.1:c.76+88C=
NM_024589.2:c.432+13C= , LRG_455t1:c.432+13C=	NP_078865.1:n.432+13C=
NR_046480.1:n.756+13C=
XM_006720947.2:c.432+13C=	XP_006721010.1:n.432+13C=
XM_006720948.2:c.162+13C=	XP_006721011.1:n.162+13C=
XM_006720947.4:c.432+13C=	XP_006721010.1:n.432+13C=
XM_006720948.4:c.162+13C=	XP_006721011.1:n.162+13C=
NM_024589.3:c.432+13C= MANE Select	NP_078865.1:n.432+13C=
NR_046480.2:n.439+13C=