Canonical Allele Identifier: CA2203529039

Gene: ROGDI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4797945C= , CM000678.2:g.4797945C=	GRCh38
NC_000016.9:g.4847946C= , CM000678.1:g.4847946C=	GRCh37
NC_000016.8:g.4787947C=	NCBI36
NG_032174.1:g.10006G= , LRG_455:g.10006G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.688G= MANE Select	ENSP00000322832.6:p.Ala230=
ENST00000322048.11:c.688G=	ENSP00000322832.5:p.Ala230=
ENST00000586153.1:c.334G=	ENSP00000464699.1:p.Ala112=
ENST00000586336.5:n.787G=
ENST00000586504.5:c.426-105G=
ENST00000587377.5:c.*8G=	ENSP00000468343.1:n.*8G=
ENST00000587711.5:c.373G=	ENSP00000467459.1:p.Ala125=
ENST00000587843.5:c.*426G=	ENSP00000465970.1:n.*426G=
ENST00000588201.5:c.*679G=	ENSP00000466529.1:n.*679G=
ENST00000589543.5:n.645G=
ENST00000591292.5:n.2017G=
ENST00000591392.5:c.616G=	ENSP00000467509.1:p.Ala206=
ENST00000592019.1:c.77-130G=
NM_024589.2:c.688G= , LRG_455t1:c.688G=	NP_078865.1:p.Ala230=
NR_046480.1:n.1012G=
XM_006720947.2:c.688G=	XP_006721010.1:p.Ala230=
XM_006720948.2:c.418G=	XP_006721011.1:p.Ala140=
XM_006720947.4:c.688G=	XP_006721010.1:p.Ala230=
XM_006720948.4:c.418G=	XP_006721011.1:p.Ala140=
NM_024589.3:c.688G= MANE Select	NP_078865.1:p.Ala230=
NR_046480.2:n.695G=