Canonical Allele Identifier: CA2203529130

Gene: ROGDI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4798058G= , CM000678.2:g.4798058G=	GRCh38
NC_000016.9:g.4848059G= , CM000678.1:g.4848059G=	GRCh37
NC_000016.8:g.4788060G=	NCBI36
NG_032174.1:g.9893C= , LRG_455:g.9893C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.645+13C= MANE Select	ENSP00000322832.6:n.645+13C=
ENST00000322048.11:c.645+13C=	ENSP00000322832.5:n.645+13C=
ENST00000586153.1:c.291+13C=	ENSP00000464699.1:n.291+13C=
ENST00000586336.5:n.744+13C=
ENST00000586504.5:c.425+13C=
ENST00000587377.5:c.658+13C=	ENSP00000468343.1:n.658+13C=
ENST00000587711.5:c.330+13C=	ENSP00000467459.1:n.330+13C=
ENST00000587843.5:c.*383+13C=	ENSP00000465970.1:n.*383+13C=
ENST00000588201.5:c.*636+13C=	ENSP00000466529.1:n.*636+13C=
ENST00000589543.5:n.602+13C=
ENST00000591292.5:n.1974+13C=
ENST00000591392.5:c.573+13C=	ENSP00000467509.1:n.573+13C=
ENST00000592019.1:c.77-243C=
NM_024589.2:c.645+13C= , LRG_455t1:c.645+13C=	NP_078865.1:n.645+13C=
NR_046480.1:n.969+13C=
XM_006720947.2:c.645+13C=	XP_006721010.1:n.645+13C=
XM_006720948.2:c.375+13C=	XP_006721011.1:n.375+13C=
XM_006720947.4:c.645+13C=	XP_006721010.1:n.645+13C=
XM_006720948.4:c.375+13C=	XP_006721011.1:n.375+13C=
NM_024589.3:c.645+13C= MANE Select	NP_078865.1:n.645+13C=
NR_046480.2:n.652+13C=