Canonical Allele Identifier: CA2203529062

Gene: ROGDI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4797974G= , CM000678.2:g.4797974G=	GRCh38
NC_000016.9:g.4847975G= , CM000678.1:g.4847975G=	GRCh37
NC_000016.8:g.4787976G=	NCBI36
NG_032174.1:g.9977C= , LRG_455:g.9977C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.659C= MANE Select	ENSP00000322832.6:p.Ala220=
ENST00000322048.11:c.659C=	ENSP00000322832.5:p.Ala220=
ENST00000586153.1:c.305C=	ENSP00000464699.1:p.Ala102=
ENST00000586336.5:n.758C=
ENST00000586504.5:c.425+97C=
ENST00000587377.5:c.672C=	ENSP00000468343.1:p.Ser224=
ENST00000587711.5:c.344C=	ENSP00000467459.1:p.Ala115=
ENST00000587843.5:c.*397C=	ENSP00000465970.1:n.*397C=
ENST00000588201.5:c.*650C=	ENSP00000466529.1:n.*650C=
ENST00000589543.5:n.616C=
ENST00000591292.5:n.1988C=
ENST00000591392.5:c.587C=	ENSP00000467509.1:p.Ala196=
ENST00000592019.1:c.77-159C=
NM_024589.2:c.659C= , LRG_455t1:c.659C=	NP_078865.1:p.Ala220=
NR_046480.1:n.983C=
XM_006720947.2:c.659C=	XP_006721010.1:p.Ala220=
XM_006720948.2:c.389C=	XP_006721011.1:p.Ala130=
XM_006720947.4:c.659C=	XP_006721010.1:p.Ala220=
XM_006720948.4:c.389C=	XP_006721011.1:p.Ala130=
NM_024589.3:c.659C= MANE Select	NP_078865.1:p.Ala220=
NR_046480.2:n.666C=