Canonical Allele Identifier: CA2203529059

Gene: ROGDI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4797972C= , CM000678.2:g.4797972C=	GRCh38
NC_000016.9:g.4847973C= , CM000678.1:g.4847973C=	GRCh37
NC_000016.8:g.4787974C=	NCBI36
NG_032174.1:g.9979G= , LRG_455:g.9979G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.661G= MANE Select	ENSP00000322832.6:p.Gly221=
ENST00000322048.11:c.661G=	ENSP00000322832.5:p.Gly221=
ENST00000586153.1:c.307G=	ENSP00000464699.1:p.Gly103=
ENST00000586336.5:n.760G=
ENST00000586504.5:c.425+99G=
ENST00000587377.5:c.674G=	ENSP00000468343.1:p.Trp225=
ENST00000587711.5:c.346G=	ENSP00000467459.1:p.Gly116=
ENST00000587843.5:c.*399G=	ENSP00000465970.1:n.*399G=
ENST00000588201.5:c.*652G=	ENSP00000466529.1:n.*652G=
ENST00000589543.5:n.618G=
ENST00000591292.5:n.1990G=
ENST00000591392.5:c.589G=	ENSP00000467509.1:p.Gly197=
ENST00000592019.1:c.77-157G=
NM_024589.2:c.661G= , LRG_455t1:c.661G=	NP_078865.1:p.Gly221=
NR_046480.1:n.985G=
XM_006720947.2:c.661G=	XP_006721010.1:p.Gly221=
XM_006720948.2:c.391G=	XP_006721011.1:p.Gly131=
XM_006720947.4:c.661G=	XP_006721010.1:p.Gly221=
XM_006720948.4:c.391G=	XP_006721011.1:p.Gly131=
NM_024589.3:c.661G= MANE Select	NP_078865.1:p.Gly221=
NR_046480.2:n.668G=