Canonical Allele Identifier: CA2203529157

Gene: ROGDI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4798088G= , CM000678.2:g.4798088G=	GRCh38
NC_000016.9:g.4848089G= , CM000678.1:g.4848089G=	GRCh37
NC_000016.8:g.4788090G=	NCBI36
NG_032174.1:g.9863C= , LRG_455:g.9863C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.628C= MANE Select	ENSP00000322832.6:p.Gln210=
ENST00000322048.11:c.628C=	ENSP00000322832.5:p.Gln210=
ENST00000586153.1:c.274C=	ENSP00000464699.1:p.Gln92=
ENST00000586336.5:n.727C=
ENST00000586504.5:c.408C=
ENST00000587377.5:c.641C=	ENSP00000468343.1:p.Ala214=
ENST00000587711.5:c.313C=	ENSP00000467459.1:p.Gln105=
ENST00000587843.5:c.*366C=	ENSP00000465970.1:n.*366C=
ENST00000588201.5:c.*619C=	ENSP00000466529.1:n.*619C=
ENST00000589543.5:n.585C=
ENST00000591292.5:n.1957C=
ENST00000591392.5:c.556C=	ENSP00000467509.1:p.Gln186=
ENST00000592019.1:c.77-273C=
NM_024589.2:c.628C= , LRG_455t1:c.628C=	NP_078865.1:p.Gln210=
NR_046480.1:n.952C=
XM_006720947.2:c.628C=	XP_006721010.1:p.Gln210=
XM_006720948.2:c.358C=	XP_006721011.1:p.Gln120=
XM_006720947.4:c.628C=	XP_006721010.1:p.Gln210=
XM_006720948.4:c.358C=	XP_006721011.1:p.Gln120=
NM_024589.3:c.628C= MANE Select	NP_078865.1:p.Gln210=
NR_046480.2:n.635C=