Canonical Allele Identifier: CA2203529064

Gene: ROGDI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4797977G= , CM000678.2:g.4797977G=	GRCh38
NC_000016.9:g.4847978G= , CM000678.1:g.4847978G=	GRCh37
NC_000016.8:g.4787979G=	NCBI36
NG_032174.1:g.9974C= , LRG_455:g.9974C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.656C= MANE Select	ENSP00000322832.6:p.Pro219=
ENST00000322048.11:c.656C=	ENSP00000322832.5:p.Pro219=
ENST00000586153.1:c.302C=	ENSP00000464699.1:p.Pro101=
ENST00000586336.5:n.755C=
ENST00000586504.5:c.425+94C=
ENST00000587377.5:c.669C=	ENSP00000468343.1:p.Pro223=
ENST00000587711.5:c.341C=	ENSP00000467459.1:p.Pro114=
ENST00000587843.5:c.*394C=	ENSP00000465970.1:n.*394C=
ENST00000588201.5:c.*647C=	ENSP00000466529.1:n.*647C=
ENST00000589543.5:n.613C=
ENST00000591292.5:n.1985C=
ENST00000591392.5:c.584C=	ENSP00000467509.1:p.Pro195=
ENST00000592019.1:c.77-162C=
NM_024589.2:c.656C= , LRG_455t1:c.656C=	NP_078865.1:p.Pro219=
NR_046480.1:n.980C=
XM_006720947.2:c.656C=	XP_006721010.1:p.Pro219=
XM_006720948.2:c.386C=	XP_006721011.1:p.Pro129=
XM_006720947.4:c.656C=	XP_006721010.1:p.Pro219=
XM_006720948.4:c.386C=	XP_006721011.1:p.Pro129=
NM_024589.3:c.656C= MANE Select	NP_078865.1:p.Pro219=
NR_046480.2:n.663C=