Canonical Allele Identifier: CA2203529048

Gene: ROGDI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4797956T= , CM000678.2:g.4797956T=	GRCh38
NC_000016.9:g.4847957T= , CM000678.1:g.4847957T=	GRCh37
NC_000016.8:g.4787958T=	NCBI36
NG_032174.1:g.9995A= , LRG_455:g.9995A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.677A= MANE Select	ENSP00000322832.6:p.His226=
ENST00000322048.11:c.677A=	ENSP00000322832.5:p.His226=
ENST00000586153.1:c.323A=	ENSP00000464699.1:p.His108=
ENST00000586336.5:n.776A=
ENST00000586504.5:c.426-116A=
ENST00000587377.5:c.690A=	ENSP00000468343.1:p.Ala230=
ENST00000587711.5:c.362A=	ENSP00000467459.1:p.His121=
ENST00000587843.5:c.*415A=	ENSP00000465970.1:n.*415A=
ENST00000588201.5:c.*668A=	ENSP00000466529.1:n.*668A=
ENST00000589543.5:n.634A=
ENST00000591292.5:n.2006A=
ENST00000591392.5:c.605A=	ENSP00000467509.1:p.His202=
ENST00000592019.1:c.77-141A=
NM_024589.2:c.677A= , LRG_455t1:c.677A=	NP_078865.1:p.His226=
NR_046480.1:n.1001A=
XM_006720947.2:c.677A=	XP_006721010.1:p.His226=
XM_006720948.2:c.407A=	XP_006721011.1:p.His136=
XM_006720947.4:c.677A=	XP_006721010.1:p.His226=
XM_006720948.4:c.407A=	XP_006721011.1:p.His136=
NM_024589.3:c.677A= MANE Select	NP_078865.1:p.His226=
NR_046480.2:n.684A=