Canonical Allele Identifier: CA2203530273

Gene: ROGDI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4799719G= , CM000678.2:g.4799719G=	GRCh38
NC_000016.9:g.4849720G= , CM000678.1:g.4849720G=	GRCh37
NC_000016.8:g.4789721G=	NCBI36
NG_032174.1:g.8232C= , LRG_455:g.8232C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.399C= MANE Select	ENSP00000322832.6:p.Ser133=
ENST00000322048.11:c.399C=	ENSP00000322832.5:p.Ser133=
ENST00000585653.1:n.531C=
ENST00000586153.1:c.144C=	ENSP00000464699.1:p.Ser48=
ENST00000586336.5:n.498C=
ENST00000586504.5:c.179C=
ENST00000587377.5:c.399C=	ENSP00000468343.1:p.Ser133=
ENST00000587711.5:c.118-1052C=	ENSP00000467459.1:n.118-1052C=
ENST00000587843.5:c.*137C=	ENSP00000465970.1:n.*137C=
ENST00000588201.5:c.*256C=	ENSP00000466529.1:n.*256C=
ENST00000589543.5:n.356C=
ENST00000591292.5:n.1728C=
ENST00000591392.5:c.327C=	ENSP00000467509.1:p.Ser109=
ENST00000592019.1:c.76+42C=
NM_024589.2:c.399C= , LRG_455t1:c.399C=	NP_078865.1:p.Ser133=
NR_046480.1:n.723C=
XM_006720947.2:c.399C=	XP_006721010.1:p.Ser133=
XM_006720948.2:c.129C=	XP_006721011.1:p.Ser43=
XM_006720947.4:c.399C=	XP_006721010.1:p.Ser133=
XM_006720948.4:c.129C=	XP_006721011.1:p.Ser43=
NM_024589.3:c.399C= MANE Select	NP_078865.1:p.Ser133=
NR_046480.2:n.406C=