Canonical Allele Identifier: CA2203530268

Gene: ROGDI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4799709T= , CM000678.2:g.4799709T=	GRCh38
NC_000016.9:g.4849710T= , CM000678.1:g.4849710T=	GRCh37
NC_000016.8:g.4789711T=	NCBI36
NG_032174.1:g.8242A= , LRG_455:g.8242A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.409A= MANE Select	ENSP00000322832.6:p.Lys137=
ENST00000322048.11:c.409A=	ENSP00000322832.5:p.Lys137=
ENST00000585653.1:n.541A=
ENST00000586153.1:c.154A=	ENSP00000464699.1:p.Lys52=
ENST00000586336.5:n.508A=
ENST00000586504.5:c.189A=
ENST00000587377.5:c.409A=	ENSP00000468343.1:p.Lys137=
ENST00000587711.5:c.118-1042A=	ENSP00000467459.1:n.118-1042A=
ENST00000587843.5:c.*147A=	ENSP00000465970.1:n.*147A=
ENST00000588201.5:c.*266A=	ENSP00000466529.1:n.*266A=
ENST00000589543.5:n.366A=
ENST00000591292.5:n.1738A=
ENST00000591392.5:c.337A=	ENSP00000467509.1:p.Lys113=
ENST00000592019.1:c.76+52A=
NM_024589.2:c.409A= , LRG_455t1:c.409A=	NP_078865.1:p.Lys137=
NR_046480.1:n.733A=
XM_006720947.2:c.409A=	XP_006721010.1:p.Lys137=
XM_006720948.2:c.139A=	XP_006721011.1:p.Lys47=
XM_006720947.4:c.409A=	XP_006721010.1:p.Lys137=
XM_006720948.4:c.139A=	XP_006721011.1:p.Lys47=
NM_024589.3:c.409A= MANE Select	NP_078865.1:p.Lys137=
NR_046480.2:n.416A=