Canonical Allele Identifier: CA2203530263

Gene: ROGDI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4799703C= , CM000678.2:g.4799703C=	GRCh38
NC_000016.9:g.4849704C= , CM000678.1:g.4849704C=	GRCh37
NC_000016.8:g.4789705C=	NCBI36
NG_032174.1:g.8248G= , LRG_455:g.8248G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.415G= MANE Select	ENSP00000322832.6:p.Gly139=
ENST00000322048.11:c.415G=	ENSP00000322832.5:p.Gly139=
ENST00000585653.1:n.547G=
ENST00000586153.1:c.160G=	ENSP00000464699.1:p.Gly54=
ENST00000586336.5:n.514G=
ENST00000586504.5:c.195G=
ENST00000587377.5:c.415G=	ENSP00000468343.1:p.Gly139=
ENST00000587711.5:c.118-1036G=	ENSP00000467459.1:n.118-1036G=
ENST00000587843.5:c.*153G=	ENSP00000465970.1:n.*153G=
ENST00000588201.5:c.*272G=	ENSP00000466529.1:n.*272G=
ENST00000589543.5:n.372G=
ENST00000591292.5:n.1744G=
ENST00000591392.5:c.343G=	ENSP00000467509.1:p.Gly115=
ENST00000592019.1:c.76+58G=
NM_024589.2:c.415G= , LRG_455t1:c.415G=	NP_078865.1:p.Gly139=
NR_046480.1:n.739G=
XM_006720947.2:c.415G=	XP_006721010.1:p.Gly139=
XM_006720948.2:c.145G=	XP_006721011.1:p.Gly49=
XM_006720947.4:c.415G=	XP_006721010.1:p.Gly139=
XM_006720948.4:c.145G=	XP_006721011.1:p.Gly49=
NM_024589.3:c.415G= MANE Select	NP_078865.1:p.Gly139=
NR_046480.2:n.422G=