Canonical Allele Identifier: CA2203529031

Gene: ROGDI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4797933C= , CM000678.2:g.4797933C=	GRCh38
NC_000016.9:g.4847934C= , CM000678.1:g.4847934C=	GRCh37
NC_000016.8:g.4787935C=	NCBI36
NG_032174.1:g.10018G= , LRG_455:g.10018G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.695+5G= MANE Select	ENSP00000322832.6:n.695+5G=
ENST00000322048.11:c.695+5G=	ENSP00000322832.5:n.695+5G=
ENST00000586153.1:c.341+5G=	ENSP00000464699.1:n.341+5G=
ENST00000586336.5:n.794+5G=
ENST00000586504.5:c.426-93G=
ENST00000587377.5:c.*15+5G=	ENSP00000468343.1:n.*15+5G=
ENST00000587711.5:c.380+5G=	ENSP00000467459.1:n.380+5G=
ENST00000587843.5:c.*433+5G=	ENSP00000465970.1:n.*433+5G=
ENST00000588201.5:c.*686+5G=	ENSP00000466529.1:n.*686+5G=
ENST00000589543.5:n.652+5G=
ENST00000591292.5:n.2024+5G=
ENST00000591392.5:c.623+5G=	ENSP00000467509.1:n.623+5G=
ENST00000592019.1:c.77-118G=
NM_024589.2:c.695+5G= , LRG_455t1:c.695+5G=	NP_078865.1:n.695+5G=
NR_046480.1:n.1019+5G=
XM_006720947.2:c.695+5G=	XP_006721010.1:n.695+5G=
XM_006720948.2:c.425+5G=	XP_006721011.1:n.425+5G=
XM_006720947.4:c.695+5G=	XP_006721010.1:n.695+5G=
XM_006720948.4:c.425+5G=	XP_006721011.1:n.425+5G=
NM_024589.3:c.695+5G= MANE Select	NP_078865.1:n.695+5G=
NR_046480.2:n.702+5G=