Canonical Allele Identifier: CA2203529072

Gene: ROGDI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4797986T= , CM000678.2:g.4797986T=	GRCh38
NC_000016.9:g.4847987T= , CM000678.1:g.4847987T=	GRCh37
NC_000016.8:g.4787988T=	NCBI36
NG_032174.1:g.9965A= , LRG_455:g.9965A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.647A= MANE Select	ENSP00000322832.6:p.Asn216=
ENST00000322048.11:c.647A=	ENSP00000322832.5:p.Asn216=
ENST00000586153.1:c.293A=	ENSP00000464699.1:p.Asn98=
ENST00000586336.5:n.746A=
ENST00000586504.5:c.425+85A=
ENST00000587377.5:c.660A=	ENSP00000468343.1:p.Glu220=
ENST00000587711.5:c.332A=	ENSP00000467459.1:p.Asn111=
ENST00000587843.5:c.*385A=	ENSP00000465970.1:n.*385A=
ENST00000588201.5:c.*638A=	ENSP00000466529.1:n.*638A=
ENST00000589543.5:n.604A=
ENST00000591292.5:n.1976A=
ENST00000591392.5:c.575A=	ENSP00000467509.1:p.Asn192=
ENST00000592019.1:c.77-171A=
NM_024589.2:c.647A= , LRG_455t1:c.647A=	NP_078865.1:p.Asn216=
NR_046480.1:n.971A=
XM_006720947.2:c.647A=	XP_006721010.1:p.Asn216=
XM_006720948.2:c.377A=	XP_006721011.1:p.Asn126=
XM_006720947.4:c.647A=	XP_006721010.1:p.Asn216=
XM_006720948.4:c.377A=	XP_006721011.1:p.Asn126=
NM_024589.3:c.647A= MANE Select	NP_078865.1:p.Asn216=
NR_046480.2:n.654A=