Canonical Allele Identifier: CA2203529051

Gene: ROGDI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4797963C= , CM000678.2:g.4797963C=	GRCh38
NC_000016.9:g.4847964C= , CM000678.1:g.4847964C=	GRCh37
NC_000016.8:g.4787965C=	NCBI36
NG_032174.1:g.9988G= , LRG_455:g.9988G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.670G= MANE Select	ENSP00000322832.6:p.Val224=
ENST00000322048.11:c.670G=	ENSP00000322832.5:p.Val224=
ENST00000586153.1:c.316G=	ENSP00000464699.1:p.Val106=
ENST00000586336.5:n.769G=
ENST00000586504.5:c.425+108G=
ENST00000587377.5:c.683G=	ENSP00000468343.1:p.Gly228=
ENST00000587711.5:c.355G=	ENSP00000467459.1:p.Val119=
ENST00000587843.5:c.*408G=	ENSP00000465970.1:n.*408G=
ENST00000588201.5:c.*661G=	ENSP00000466529.1:n.*661G=
ENST00000589543.5:n.627G=
ENST00000591292.5:n.1999G=
ENST00000591392.5:c.598G=	ENSP00000467509.1:p.Val200=
ENST00000592019.1:c.77-148G=
NM_024589.2:c.670G= , LRG_455t1:c.670G=	NP_078865.1:p.Val224=
NR_046480.1:n.994G=
XM_006720947.2:c.670G=	XP_006721010.1:p.Val224=
XM_006720948.2:c.400G=	XP_006721011.1:p.Val134=
XM_006720947.4:c.670G=	XP_006721010.1:p.Val224=
XM_006720948.4:c.400G=	XP_006721011.1:p.Val134=
NM_024589.3:c.670G= MANE Select	NP_078865.1:p.Val224=
NR_046480.2:n.677G=