Canonical Allele Identifier: CA2203530293

Gene: ROGDI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4799751C= , CM000678.2:g.4799751C=	GRCh38
NC_000016.9:g.4849752C= , CM000678.1:g.4849752C=	GRCh37
NC_000016.8:g.4789753C=	NCBI36
NG_032174.1:g.8200G= , LRG_455:g.8200G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.367G= MANE Select	ENSP00000322832.6:p.Ala123=
ENST00000322048.11:c.367G=	ENSP00000322832.5:p.Ala123=
ENST00000585653.1:n.499G=
ENST00000586153.1:c.112G=	ENSP00000464699.1:p.Ala38=
ENST00000586336.5:n.466G=
ENST00000586504.5:c.147G=
ENST00000587377.5:c.367G=	ENSP00000468343.1:p.Ala123=
ENST00000587711.5:c.118-1084G=	ENSP00000467459.1:n.118-1084G=
ENST00000587843.5:c.*105G=	ENSP00000465970.1:n.*105G=
ENST00000588201.5:c.*224G=	ENSP00000466529.1:n.*224G=
ENST00000589543.5:n.324G=
ENST00000591292.5:n.1696G=
ENST00000591392.5:c.295G=	ENSP00000467509.1:p.Ala99=
ENST00000592019.1:c.76+10G=
NM_024589.2:c.367G= , LRG_455t1:c.367G=	NP_078865.1:p.Ala123=
NR_046480.1:n.691G=
XM_006720947.2:c.367G=	XP_006721010.1:p.Ala123=
XM_006720948.2:c.97G=	XP_006721011.1:p.Ala33=
XM_006720947.4:c.367G=	XP_006721010.1:p.Ala123=
XM_006720948.4:c.97G=	XP_006721011.1:p.Ala33=
NM_024589.3:c.367G= MANE Select	NP_078865.1:p.Ala123=
NR_046480.2:n.374G=