Canonical Allele Identifier: CA2203529149

Gene: ROGDI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4798072T= , CM000678.2:g.4798072T=	GRCh38
NC_000016.9:g.4848073T= , CM000678.1:g.4848073T=	GRCh37
NC_000016.8:g.4788074T=	NCBI36
NG_032174.1:g.9879A= , LRG_455:g.9879A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.644A= MANE Select	ENSP00000322832.6:p.Lys215=
ENST00000322048.11:c.644A=	ENSP00000322832.5:p.Lys215=
ENST00000586153.1:c.290A=	ENSP00000464699.1:p.Lys97=
ENST00000586336.5:n.743A=
ENST00000586504.5:c.424A=
ENST00000587377.5:c.657A=	ENSP00000468343.1:p.Gln219=
ENST00000587711.5:c.329A=	ENSP00000467459.1:p.Lys110=
ENST00000587843.5:c.*382A=	ENSP00000465970.1:n.*382A=
ENST00000588201.5:c.*635A=	ENSP00000466529.1:n.*635A=
ENST00000589543.5:n.601A=
ENST00000591292.5:n.1973A=
ENST00000591392.5:c.572A=	ENSP00000467509.1:p.Lys191=
ENST00000592019.1:c.77-257A=
NM_024589.2:c.644A= , LRG_455t1:c.644A=	NP_078865.1:p.Lys215=
NR_046480.1:n.968A=
XM_006720947.2:c.644A=	XP_006721010.1:p.Lys215=
XM_006720948.2:c.374A=	XP_006721011.1:p.Lys125=
XM_006720947.4:c.644A=	XP_006721010.1:p.Lys215=
XM_006720948.4:c.374A=	XP_006721011.1:p.Lys125=
NM_024589.3:c.644A= MANE Select	NP_078865.1:p.Lys215=
NR_046480.2:n.651A=