Canonical Allele Identifier: CA2203529058

Gene: ROGDI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4797970C= , CM000678.2:g.4797970C=	GRCh38
NC_000016.9:g.4847971C= , CM000678.1:g.4847971C=	GRCh37
NC_000016.8:g.4787972C=	NCBI36
NG_032174.1:g.9981G= , LRG_455:g.9981G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.663G= MANE Select	ENSP00000322832.6:p.Gly221=
ENST00000322048.11:c.663G=	ENSP00000322832.5:p.Gly221=
ENST00000586153.1:c.309G=	ENSP00000464699.1:p.Gly103=
ENST00000586336.5:n.762G=
ENST00000586504.5:c.425+101G=
ENST00000587377.5:c.676G=	ENSP00000468343.1:p.Gly226=
ENST00000587711.5:c.348G=	ENSP00000467459.1:p.Gly116=
ENST00000587843.5:c.*401G=	ENSP00000465970.1:n.*401G=
ENST00000588201.5:c.*654G=	ENSP00000466529.1:n.*654G=
ENST00000589543.5:n.620G=
ENST00000591292.5:n.1992G=
ENST00000591392.5:c.591G=	ENSP00000467509.1:p.Gly197=
ENST00000592019.1:c.77-155G=
NM_024589.2:c.663G= , LRG_455t1:c.663G=	NP_078865.1:p.Gly221=
NR_046480.1:n.987G=
XM_006720947.2:c.663G=	XP_006721010.1:p.Gly221=
XM_006720948.2:c.393G=	XP_006721011.1:p.Gly131=
XM_006720947.4:c.663G=	XP_006721010.1:p.Gly221=
XM_006720948.4:c.393G=	XP_006721011.1:p.Gly131=
NM_024589.3:c.663G= MANE Select	NP_078865.1:p.Gly221=
NR_046480.2:n.670G=