Canonical Allele Identifier: CA2203530299

Gene: ROGDI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4799770G= , CM000678.2:g.4799770G=	GRCh38
NC_000016.9:g.4849771G= , CM000678.1:g.4849771G=	GRCh37
NC_000016.8:g.4789772G=	NCBI36
NG_032174.1:g.8181C= , LRG_455:g.8181C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.348C= MANE Select	ENSP00000322832.6:p.Ala116=
ENST00000322048.11:c.348C=	ENSP00000322832.5:p.Ala116=
ENST00000585653.1:n.480C=
ENST00000586153.1:c.93C=	ENSP00000464699.1:p.Ala31=
ENST00000586336.5:n.447C=
ENST00000586504.5:c.128C=
ENST00000587377.5:c.348C=	ENSP00000468343.1:p.Ala116=
ENST00000587711.5:c.118-1103C=	ENSP00000467459.1:n.118-1103C=
ENST00000587843.5:c.*86C=	ENSP00000465970.1:n.*86C=
ENST00000588201.5:c.*205C=	ENSP00000466529.1:n.*205C=
ENST00000589543.5:n.305C=
ENST00000591292.5:n.1677C=
ENST00000591392.5:c.276C=	ENSP00000467509.1:p.Ala92=
ENST00000592019.1:c.67C=
NM_024589.2:c.348C= , LRG_455t1:c.348C=	NP_078865.1:p.Ala116=
NR_046480.1:n.672C=
XM_006720947.2:c.348C=	XP_006721010.1:p.Ala116=
XM_006720948.2:c.78C=	XP_006721011.1:p.Ala26=
XM_006720947.4:c.348C=	XP_006721010.1:p.Ala116=
XM_006720948.4:c.78C=	XP_006721011.1:p.Ala26=
NM_024589.3:c.348C= MANE Select	NP_078865.1:p.Ala116=
NR_046480.2:n.355C=