Canonical Allele Identifier: CA2203529178

Gene: ROGDI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4798112T= , CM000678.2:g.4798112T=	GRCh38
NC_000016.9:g.4848113T= , CM000678.1:g.4848113T=	GRCh37
NC_000016.8:g.4788114T=	NCBI36
NG_032174.1:g.9839A= , LRG_455:g.9839A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.604A= MANE Select	ENSP00000322832.6:p.Thr202=
ENST00000322048.11:c.604A=	ENSP00000322832.5:p.Thr202=
ENST00000586153.1:c.250A=	ENSP00000464699.1:p.Thr84=
ENST00000586336.5:n.703A=
ENST00000586504.5:c.384A=
ENST00000587377.5:c.617A=	ENSP00000468343.1:p.His206=
ENST00000587711.5:c.289A=	ENSP00000467459.1:p.Thr97=
ENST00000587843.5:c.*342A=	ENSP00000465970.1:n.*342A=
ENST00000588201.5:c.*595A=	ENSP00000466529.1:n.*595A=
ENST00000589543.5:n.561A=
ENST00000591292.5:n.1933A=
ENST00000591392.5:c.532A=	ENSP00000467509.1:p.Thr178=
ENST00000592019.1:c.77-297A=
NM_024589.2:c.604A= , LRG_455t1:c.604A=	NP_078865.1:p.Thr202=
NR_046480.1:n.928A=
XM_006720947.2:c.604A=	XP_006721010.1:p.Thr202=
XM_006720948.2:c.334A=	XP_006721011.1:p.Thr112=
XM_006720947.4:c.604A=	XP_006721010.1:p.Thr202=
XM_006720948.4:c.334A=	XP_006721011.1:p.Thr112=
NM_024589.3:c.604A= MANE Select	NP_078865.1:p.Thr202=
NR_046480.2:n.611A=