Canonical Allele Identifier: CA2203529098

Gene: ROGDI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4798026G= , CM000678.2:g.4798026G=	GRCh38
NC_000016.9:g.4848027G= , CM000678.1:g.4848027G=	GRCh37
NC_000016.8:g.4788028G=	NCBI36
NG_032174.1:g.9925C= , LRG_455:g.9925C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.646-39C= MANE Select	ENSP00000322832.6:n.646-39C=
ENST00000322048.11:c.646-39C=	ENSP00000322832.5:n.646-39C=
ENST00000586153.1:c.292-39C=	ENSP00000464699.1:n.292-39C=
ENST00000586336.5:n.745-39C=
ENST00000586504.5:c.425+45C=
ENST00000587377.5:c.659-39C=	ENSP00000468343.1:n.659-39C=
ENST00000587711.5:c.331-39C=	ENSP00000467459.1:n.331-39C=
ENST00000587843.5:c.*384-39C=	ENSP00000465970.1:n.*384-39C=
ENST00000588201.5:c.*637-39C=	ENSP00000466529.1:n.*637-39C=
ENST00000589543.5:n.603-39C=
ENST00000591292.5:n.1975-39C=
ENST00000591392.5:c.574-39C=	ENSP00000467509.1:n.574-39C=
ENST00000592019.1:c.77-211C=
NM_024589.2:c.646-39C= , LRG_455t1:c.646-39C=	NP_078865.1:n.646-39C=
NR_046480.1:n.970-39C=
XM_006720947.2:c.646-39C=	XP_006721010.1:n.646-39C=
XM_006720948.2:c.376-39C=	XP_006721011.1:n.376-39C=
XM_006720947.4:c.646-39C=	XP_006721010.1:n.646-39C=
XM_006720948.4:c.376-39C=	XP_006721011.1:n.376-39C=
NM_024589.3:c.646-39C= MANE Select	NP_078865.1:n.646-39C=
NR_046480.2:n.653-39C=