Canonical Allele Identifier: CA2203529063

Gene: ROGDI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4797975C= , CM000678.2:g.4797975C=	GRCh38
NC_000016.9:g.4847976C= , CM000678.1:g.4847976C=	GRCh37
NC_000016.8:g.4787977C=	NCBI36
NG_032174.1:g.9976G= , LRG_455:g.9976G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.658G= MANE Select	ENSP00000322832.6:p.Ala220=
ENST00000322048.11:c.658G=	ENSP00000322832.5:p.Ala220=
ENST00000586153.1:c.304G=	ENSP00000464699.1:p.Ala102=
ENST00000586336.5:n.757G=
ENST00000586504.5:c.425+96G=
ENST00000587377.5:c.671G=	ENSP00000468343.1:p.Ser224=
ENST00000587711.5:c.343G=	ENSP00000467459.1:p.Ala115=
ENST00000587843.5:c.*396G=	ENSP00000465970.1:n.*396G=
ENST00000588201.5:c.*649G=	ENSP00000466529.1:n.*649G=
ENST00000589543.5:n.615G=
ENST00000591292.5:n.1987G=
ENST00000591392.5:c.586G=	ENSP00000467509.1:p.Ala196=
ENST00000592019.1:c.77-160G=
NM_024589.2:c.658G= , LRG_455t1:c.658G=	NP_078865.1:p.Ala220=
NR_046480.1:n.982G=
XM_006720947.2:c.658G=	XP_006721010.1:p.Ala220=
XM_006720948.2:c.388G=	XP_006721011.1:p.Ala130=
XM_006720947.4:c.658G=	XP_006721010.1:p.Ala220=
XM_006720948.4:c.388G=	XP_006721011.1:p.Ala130=
NM_024589.3:c.658G= MANE Select	NP_078865.1:p.Ala220=
NR_046480.2:n.665G=