Canonical Allele Identifier: CA2203530287

Gene: ROGDI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4799742G= , CM000678.2:g.4799742G=	GRCh38
NC_000016.9:g.4849743G= , CM000678.1:g.4849743G=	GRCh37
NC_000016.8:g.4789744G=	NCBI36
NG_032174.1:g.8209C= , LRG_455:g.8209C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.376C= MANE Select	ENSP00000322832.6:p.Leu126=
ENST00000322048.11:c.376C=	ENSP00000322832.5:p.Leu126=
ENST00000585653.1:n.508C=
ENST00000586153.1:c.121C=	ENSP00000464699.1:p.Leu41=
ENST00000586336.5:n.475C=
ENST00000586504.5:c.156C=
ENST00000587377.5:c.376C=	ENSP00000468343.1:p.Leu126=
ENST00000587711.5:c.118-1075C=	ENSP00000467459.1:n.118-1075C=
ENST00000587843.5:c.*114C=	ENSP00000465970.1:n.*114C=
ENST00000588201.5:c.*233C=	ENSP00000466529.1:n.*233C=
ENST00000589543.5:n.333C=
ENST00000591292.5:n.1705C=
ENST00000591392.5:c.304C=	ENSP00000467509.1:p.Leu102=
ENST00000592019.1:c.76+19C=
NM_024589.2:c.376C= , LRG_455t1:c.376C=	NP_078865.1:p.Leu126=
NR_046480.1:n.700C=
XM_006720947.2:c.376C=	XP_006721010.1:p.Leu126=
XM_006720948.2:c.106C=	XP_006721011.1:p.Leu36=
XM_006720947.4:c.376C=	XP_006721010.1:p.Leu126=
XM_006720948.4:c.106C=	XP_006721011.1:p.Leu36=
NM_024589.3:c.376C= MANE Select	NP_078865.1:p.Leu126=
NR_046480.2:n.383C=