Canonical Allele Identifier: CA2203529216

Gene: ROGDI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4798170A= , CM000678.2:g.4798170A=	GRCh38
NC_000016.9:g.4848171A= , CM000678.1:g.4848171A=	GRCh37
NC_000016.8:g.4788172A=	NCBI36
NG_032174.1:g.9781T= , LRG_455:g.9781T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.546T= MANE Select	ENSP00000322832.6:p.Pro182=
ENST00000322048.11:c.546T=	ENSP00000322832.5:p.Pro182=
ENST00000586153.1:c.192T=	ENSP00000464699.1:p.Pro64=
ENST00000586336.5:n.645T=
ENST00000586504.5:c.326T=
ENST00000587377.5:c.559T=	ENSP00000468343.1:p.Cys187=
ENST00000587711.5:c.231T=	ENSP00000467459.1:p.Pro77=
ENST00000587843.5:c.*284T=	ENSP00000465970.1:n.*284T=
ENST00000588201.5:c.*537T=	ENSP00000466529.1:n.*537T=
ENST00000589543.5:n.503T=
ENST00000591292.5:n.1875T=
ENST00000591392.5:c.474T=	ENSP00000467509.1:p.Pro158=
ENST00000592019.1:c.77-355T=
NM_024589.2:c.546T= , LRG_455t1:c.546T=	NP_078865.1:p.Pro182=
NR_046480.1:n.870T=
XM_006720947.2:c.546T=	XP_006721010.1:p.Pro182=
XM_006720948.2:c.276T=	XP_006721011.1:p.Pro92=
XM_006720947.4:c.546T=	XP_006721010.1:p.Pro182=
XM_006720948.4:c.276T=	XP_006721011.1:p.Pro92=
NM_024589.3:c.546T= MANE Select	NP_078865.1:p.Pro182=
NR_046480.2:n.553T=