Canonical Allele Identifier: CA2203529071

Gene: ROGDI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4797985G= , CM000678.2:g.4797985G=	GRCh38
NC_000016.9:g.4847986G= , CM000678.1:g.4847986G=	GRCh37
NC_000016.8:g.4787987G=	NCBI36
NG_032174.1:g.9966C= , LRG_455:g.9966C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.648C= MANE Select	ENSP00000322832.6:p.Asn216=
ENST00000322048.11:c.648C=	ENSP00000322832.5:p.Asn216=
ENST00000586153.1:c.294C=	ENSP00000464699.1:p.Asn98=
ENST00000586336.5:n.747C=
ENST00000586504.5:c.425+86C=
ENST00000587377.5:c.661C=	ENSP00000468343.1:p.Leu221=
ENST00000587711.5:c.333C=	ENSP00000467459.1:p.Asn111=
ENST00000587843.5:c.*386C=	ENSP00000465970.1:n.*386C=
ENST00000588201.5:c.*639C=	ENSP00000466529.1:n.*639C=
ENST00000589543.5:n.605C=
ENST00000591292.5:n.1977C=
ENST00000591392.5:c.576C=	ENSP00000467509.1:p.Asn192=
ENST00000592019.1:c.77-170C=
NM_024589.2:c.648C= , LRG_455t1:c.648C=	NP_078865.1:p.Asn216=
NR_046480.1:n.972C=
XM_006720947.2:c.648C=	XP_006721010.1:p.Asn216=
XM_006720948.2:c.378C=	XP_006721011.1:p.Asn126=
XM_006720947.4:c.648C=	XP_006721010.1:p.Asn216=
XM_006720948.4:c.378C=	XP_006721011.1:p.Asn126=
NM_024589.3:c.648C= MANE Select	NP_078865.1:p.Asn216=
NR_046480.2:n.655C=