Canonical Allele Identifier: CA2203529033

Gene: ROGDI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4797938A= , CM000678.2:g.4797938A=	GRCh38
NC_000016.9:g.4847939A= , CM000678.1:g.4847939A=	GRCh37
NC_000016.8:g.4787940A=	NCBI36
NG_032174.1:g.10013T= , LRG_455:g.10013T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.695T= MANE Select	ENSP00000322832.6:p.Phe232=
ENST00000322048.11:c.695T=	ENSP00000322832.5:p.Phe232=
ENST00000586153.1:c.341T=	ENSP00000464699.1:p.Phe114=
ENST00000586336.5:n.794T=
ENST00000586504.5:c.426-98T=
ENST00000587377.5:c.*15T=	ENSP00000468343.1:n.*15T=
ENST00000587711.5:c.380T=	ENSP00000467459.1:p.Phe127=
ENST00000587843.5:c.*433T=	ENSP00000465970.1:n.*433T=
ENST00000588201.5:c.*686T=	ENSP00000466529.1:n.*686T=
ENST00000589543.5:n.652T=
ENST00000591292.5:n.2024T=
ENST00000591392.5:c.623T=	ENSP00000467509.1:p.Phe208=
ENST00000592019.1:c.77-123T=
NM_024589.2:c.695T= , LRG_455t1:c.695T=	NP_078865.1:p.Phe232=
NR_046480.1:n.1019T=
XM_006720947.2:c.695T=	XP_006721010.1:p.Leu232=
XM_006720948.2:c.425T=	XP_006721011.1:p.Leu142=
XM_006720947.4:c.695T=	XP_006721010.1:p.Leu232=
XM_006720948.4:c.425T=	XP_006721011.1:p.Leu142=
NM_024589.3:c.695T= MANE Select	NP_078865.1:p.Phe232=
NR_046480.2:n.702T=