Canonical Allele Identifier: CA2203529054

Gene: ROGDI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4797966C= , CM000678.2:g.4797966C=	GRCh38
NC_000016.9:g.4847967C= , CM000678.1:g.4847967C=	GRCh37
NC_000016.8:g.4787968C=	NCBI36
NG_032174.1:g.9985G= , LRG_455:g.9985G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.667G= MANE Select	ENSP00000322832.6:p.Ala223=
ENST00000322048.11:c.667G=	ENSP00000322832.5:p.Ala223=
ENST00000586153.1:c.313G=	ENSP00000464699.1:p.Ala105=
ENST00000586336.5:n.766G=
ENST00000586504.5:c.425+105G=
ENST00000587377.5:c.680G=	ENSP00000468343.1:p.Arg227=
ENST00000587711.5:c.352G=	ENSP00000467459.1:p.Ala118=
ENST00000587843.5:c.*405G=	ENSP00000465970.1:n.*405G=
ENST00000588201.5:c.*658G=	ENSP00000466529.1:n.*658G=
ENST00000589543.5:n.624G=
ENST00000591292.5:n.1996G=
ENST00000591392.5:c.595G=	ENSP00000467509.1:p.Ala199=
ENST00000592019.1:c.77-151G=
NM_024589.2:c.667G= , LRG_455t1:c.667G=	NP_078865.1:p.Ala223=
NR_046480.1:n.991G=
XM_006720947.2:c.667G=	XP_006721010.1:p.Ala223=
XM_006720948.2:c.397G=	XP_006721011.1:p.Ala133=
XM_006720947.4:c.667G=	XP_006721010.1:p.Ala223=
XM_006720948.4:c.397G=	XP_006721011.1:p.Ala133=
NM_024589.3:c.667G= MANE Select	NP_078865.1:p.Ala223=
NR_046480.2:n.674G=