Canonical Allele Identifier: CA2203530277

Gene: ROGDI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4799725G= , CM000678.2:g.4799725G=	GRCh38
NC_000016.9:g.4849726G= , CM000678.1:g.4849726G=	GRCh37
NC_000016.8:g.4789727G=	NCBI36
NG_032174.1:g.8226C= , LRG_455:g.8226C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.393C= MANE Select	ENSP00000322832.6:p.Asp131=
ENST00000322048.11:c.393C=	ENSP00000322832.5:p.Asp131=
ENST00000585653.1:n.525C=
ENST00000586153.1:c.138C=	ENSP00000464699.1:p.Asp46=
ENST00000586336.5:n.492C=
ENST00000586504.5:c.173C=
ENST00000587377.5:c.393C=	ENSP00000468343.1:p.Asp131=
ENST00000587711.5:c.118-1058C=	ENSP00000467459.1:n.118-1058C=
ENST00000587843.5:c.*131C=	ENSP00000465970.1:n.*131C=
ENST00000588201.5:c.*250C=	ENSP00000466529.1:n.*250C=
ENST00000589543.5:n.350C=
ENST00000591292.5:n.1722C=
ENST00000591392.5:c.321C=	ENSP00000467509.1:p.Asp107=
ENST00000592019.1:c.76+36C=
NM_024589.2:c.393C= , LRG_455t1:c.393C=	NP_078865.1:p.Asp131=
NR_046480.1:n.717C=
XM_006720947.2:c.393C=	XP_006721010.1:p.Asp131=
XM_006720948.2:c.123C=	XP_006721011.1:p.Asp41=
XM_006720947.4:c.393C=	XP_006721010.1:p.Asp131=
XM_006720948.4:c.123C=	XP_006721011.1:p.Asp41=
NM_024589.3:c.393C= MANE Select	NP_078865.1:p.Asp131=
NR_046480.2:n.400C=