Canonical Allele Identifier: CA2203529042

Gene: ROGDI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4797948C= , CM000678.2:g.4797948C=	GRCh38
NC_000016.9:g.4847949C= , CM000678.1:g.4847949C=	GRCh37
NC_000016.8:g.4787950C=	NCBI36
NG_032174.1:g.10003G= , LRG_455:g.10003G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.685G= MANE Select	ENSP00000322832.6:p.Gly229=
ENST00000322048.11:c.685G=	ENSP00000322832.5:p.Gly229=
ENST00000586153.1:c.331G=	ENSP00000464699.1:p.Gly111=
ENST00000586336.5:n.784G=
ENST00000586504.5:c.426-108G=
ENST00000587377.5:c.*5G=	ENSP00000468343.1:n.*5G=
ENST00000587711.5:c.370G=	ENSP00000467459.1:p.Gly124=
ENST00000587843.5:c.*423G=	ENSP00000465970.1:n.*423G=
ENST00000588201.5:c.*676G=	ENSP00000466529.1:n.*676G=
ENST00000589543.5:n.642G=
ENST00000591292.5:n.2014G=
ENST00000591392.5:c.613G=	ENSP00000467509.1:p.Gly205=
ENST00000592019.1:c.77-133G=
NM_024589.2:c.685G= , LRG_455t1:c.685G=	NP_078865.1:p.Gly229=
NR_046480.1:n.1009G=
XM_006720947.2:c.685G=	XP_006721010.1:p.Gly229=
XM_006720948.2:c.415G=	XP_006721011.1:p.Gly139=
XM_006720947.4:c.685G=	XP_006721010.1:p.Gly229=
XM_006720948.4:c.415G=	XP_006721011.1:p.Gly139=
NM_024589.3:c.685G= MANE Select	NP_078865.1:p.Gly229=
NR_046480.2:n.692G=