Canonical Allele Identifier: CA2203528973

Gene: ROGDI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4797868A= , CM000678.2:g.4797868A=	GRCh38
NC_000016.9:g.4847869A= , CM000678.1:g.4847869A=	GRCh37
NC_000016.8:g.4787870A=	NCBI36
NG_032174.1:g.10083T= , LRG_455:g.10083T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.696-28T= MANE Select	ENSP00000322832.6:n.696-28T=
ENST00000322048.11:c.696-28T=	ENSP00000322832.5:n.696-28T=
ENST00000586153.1:c.342-32T=	ENSP00000464699.1:n.342-32T=
ENST00000586336.5:n.795-28T=
ENST00000586504.5:c.426-28T=
ENST00000587377.5:c.*16-28T=	ENSP00000468343.1:n.*16-28T=
ENST00000587711.5:c.381-28T=	ENSP00000467459.1:n.381-28T=
ENST00000587843.5:c.*434-28T=	ENSP00000465970.1:n.*434-28T=
ENST00000588201.5:c.*687-28T=	ENSP00000466529.1:n.*687-28T=
ENST00000589543.5:n.653-28T=
ENST00000591292.5:n.2025-28T=
ENST00000591392.5:c.624-28T=	ENSP00000467509.1:n.624-28T=
ENST00000592019.1:c.77-53T=
NM_024589.2:c.696-28T= , LRG_455t1:c.696-28T=	NP_078865.1:n.696-28T=
NR_046480.1:n.1020-28T=
XM_006720947.2:c.696-7T=	XP_006721010.1:n.696-7T=
XM_006720948.2:c.426-7T=	XP_006721011.1:n.426-7T=
XM_006720947.4:c.696-7T=	XP_006721010.1:n.696-7T=
XM_006720948.4:c.426-7T=	XP_006721011.1:n.426-7T=
NM_024589.3:c.696-28T= MANE Select	NP_078865.1:n.696-28T=
NR_046480.2:n.703-28T=