Canonical Allele Identifier: CA2203529041

Gene: ROGDI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4797947C= , CM000678.2:g.4797947C=	GRCh38
NC_000016.9:g.4847948C= , CM000678.1:g.4847948C=	GRCh37
NC_000016.8:g.4787949C=	NCBI36
NG_032174.1:g.10004G= , LRG_455:g.10004G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.686G= MANE Select	ENSP00000322832.6:p.Gly229=
ENST00000322048.11:c.686G=	ENSP00000322832.5:p.Gly229=
ENST00000586153.1:c.332G=	ENSP00000464699.1:p.Gly111=
ENST00000586336.5:n.785G=
ENST00000586504.5:c.426-107G=
ENST00000587377.5:c.*6G=	ENSP00000468343.1:n.*6G=
ENST00000587711.5:c.371G=	ENSP00000467459.1:p.Gly124=
ENST00000587843.5:c.*424G=	ENSP00000465970.1:n.*424G=
ENST00000588201.5:c.*677G=	ENSP00000466529.1:n.*677G=
ENST00000589543.5:n.643G=
ENST00000591292.5:n.2015G=
ENST00000591392.5:c.614G=	ENSP00000467509.1:p.Gly205=
ENST00000592019.1:c.77-132G=
NM_024589.2:c.686G= , LRG_455t1:c.686G=	NP_078865.1:p.Gly229=
NR_046480.1:n.1010G=
XM_006720947.2:c.686G=	XP_006721010.1:p.Gly229=
XM_006720948.2:c.416G=	XP_006721011.1:p.Gly139=
XM_006720947.4:c.686G=	XP_006721010.1:p.Gly229=
XM_006720948.4:c.416G=	XP_006721011.1:p.Gly139=
NM_024589.3:c.686G= MANE Select	NP_078865.1:p.Gly229=
NR_046480.2:n.693G=