Canonical Allele Identifier: CA2203530278

Gene: ROGDI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4799726T= , CM000678.2:g.4799726T=	GRCh38
NC_000016.9:g.4849727T= , CM000678.1:g.4849727T=	GRCh37
NC_000016.8:g.4789728T=	NCBI36
NG_032174.1:g.8225A= , LRG_455:g.8225A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.392A= MANE Select	ENSP00000322832.6:p.Asp131=
ENST00000322048.11:c.392A=	ENSP00000322832.5:p.Asp131=
ENST00000585653.1:n.524A=
ENST00000586153.1:c.137A=	ENSP00000464699.1:p.Asp46=
ENST00000586336.5:n.491A=
ENST00000586504.5:c.172A=
ENST00000587377.5:c.392A=	ENSP00000468343.1:p.Asp131=
ENST00000587711.5:c.118-1059A=	ENSP00000467459.1:n.118-1059A=
ENST00000587843.5:c.*130A=	ENSP00000465970.1:n.*130A=
ENST00000588201.5:c.*249A=	ENSP00000466529.1:n.*249A=
ENST00000589543.5:n.349A=
ENST00000591292.5:n.1721A=
ENST00000591392.5:c.320A=	ENSP00000467509.1:p.Asp107=
ENST00000592019.1:c.76+35A=
NM_024589.2:c.392A= , LRG_455t1:c.392A=	NP_078865.1:p.Asp131=
NR_046480.1:n.716A=
XM_006720947.2:c.392A=	XP_006721010.1:p.Asp131=
XM_006720948.2:c.122A=	XP_006721011.1:p.Asp41=
XM_006720947.4:c.392A=	XP_006721010.1:p.Asp131=
XM_006720948.4:c.122A=	XP_006721011.1:p.Asp41=
NM_024589.3:c.392A= MANE Select	NP_078865.1:p.Asp131=
NR_046480.2:n.399A=