Canonical Allele Identifier: CA2203529055

Gene: ROGDI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4797967G= , CM000678.2:g.4797967G=	GRCh38
NC_000016.9:g.4847968G= , CM000678.1:g.4847968G=	GRCh37
NC_000016.8:g.4787969G=	NCBI36
NG_032174.1:g.9984C= , LRG_455:g.9984C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.666C= MANE Select	ENSP00000322832.6:p.Gly222=
ENST00000322048.11:c.666C=	ENSP00000322832.5:p.Gly222=
ENST00000586153.1:c.312C=	ENSP00000464699.1:p.Gly104=
ENST00000586336.5:n.765C=
ENST00000586504.5:c.425+104C=
ENST00000587377.5:c.679C=	ENSP00000468343.1:p.Arg227=
ENST00000587711.5:c.351C=	ENSP00000467459.1:p.Gly117=
ENST00000587843.5:c.*404C=	ENSP00000465970.1:n.*404C=
ENST00000588201.5:c.*657C=	ENSP00000466529.1:n.*657C=
ENST00000589543.5:n.623C=
ENST00000591292.5:n.1995C=
ENST00000591392.5:c.594C=	ENSP00000467509.1:p.Gly198=
ENST00000592019.1:c.77-152C=
NM_024589.2:c.666C= , LRG_455t1:c.666C=	NP_078865.1:p.Gly222=
NR_046480.1:n.990C=
XM_006720947.2:c.666C=	XP_006721010.1:p.Gly222=
XM_006720948.2:c.396C=	XP_006721011.1:p.Gly132=
XM_006720947.4:c.666C=	XP_006721010.1:p.Gly222=
XM_006720948.4:c.396C=	XP_006721011.1:p.Gly132=
NM_024589.3:c.666C= MANE Select	NP_078865.1:p.Gly222=
NR_046480.2:n.673C=