Canonical Allele Identifier: CA2203530227

Gene: ROGDI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4799657C= , CM000678.2:g.4799657C=	GRCh38
NC_000016.9:g.4849658C= , CM000678.1:g.4849658C=	GRCh37
NC_000016.8:g.4789659C=	NCBI36
NG_032174.1:g.8294G= , LRG_455:g.8294G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.432+29G= MANE Select	ENSP00000322832.6:n.432+29G=
ENST00000322048.11:c.432+29G=	ENSP00000322832.5:n.432+29G=
ENST00000585653.1:n.564+29G=
ENST00000586153.1:c.177+29G=	ENSP00000464699.1:n.177+29G=
ENST00000586336.5:n.531+29G=
ENST00000586504.5:c.212+29G=
ENST00000587377.5:c.423+38G=	ENSP00000468343.1:n.423+38G=
ENST00000587711.5:c.118-990G=	ENSP00000467459.1:n.118-990G=
ENST00000587843.5:c.*170+29G=	ENSP00000465970.1:n.*170+29G=
ENST00000588201.5:c.*289+29G=	ENSP00000466529.1:n.*289+29G=
ENST00000589543.5:n.389+29G=
ENST00000591292.5:n.1761+29G=
ENST00000591392.5:c.360+29G=	ENSP00000467509.1:n.360+29G=
ENST00000592019.1:c.76+104G=
NM_024589.2:c.432+29G= , LRG_455t1:c.432+29G=	NP_078865.1:n.432+29G=
NR_046480.1:n.756+29G=
XM_006720947.2:c.432+29G=	XP_006721010.1:n.432+29G=
XM_006720948.2:c.162+29G=	XP_006721011.1:n.162+29G=
XM_006720947.4:c.432+29G=	XP_006721010.1:n.432+29G=
XM_006720948.4:c.162+29G=	XP_006721011.1:n.162+29G=
NM_024589.3:c.432+29G= MANE Select	NP_078865.1:n.432+29G=
NR_046480.2:n.439+29G=