Canonical Allele Identifier: CA2203528984

Gene: ROGDI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4797882C= , CM000678.2:g.4797882C=	GRCh38
NC_000016.9:g.4847883C= , CM000678.1:g.4847883C=	GRCh37
NC_000016.8:g.4787884C=	NCBI36
NG_032174.1:g.10069G= , LRG_455:g.10069G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.696-42G= MANE Select	ENSP00000322832.6:n.696-42G=
ENST00000322048.11:c.696-42G=	ENSP00000322832.5:n.696-42G=
ENST00000586153.1:c.342-46G=	ENSP00000464699.1:n.342-46G=
ENST00000586336.5:n.795-42G=
ENST00000586504.5:c.426-42G=
ENST00000587377.5:c.*16-42G=	ENSP00000468343.1:n.*16-42G=
ENST00000587711.5:c.381-42G=	ENSP00000467459.1:n.381-42G=
ENST00000587843.5:c.*434-42G=	ENSP00000465970.1:n.*434-42G=
ENST00000588201.5:c.*687-42G=	ENSP00000466529.1:n.*687-42G=
ENST00000589543.5:n.653-42G=
ENST00000591292.5:n.2025-42G=
ENST00000591392.5:c.624-42G=	ENSP00000467509.1:n.624-42G=
ENST00000592019.1:c.77-67G=
NM_024589.2:c.696-42G= , LRG_455t1:c.696-42G=	NP_078865.1:n.696-42G=
NR_046480.1:n.1020-42G=
XM_006720947.2:c.696-21G=	XP_006721010.1:n.696-21G=
XM_006720948.2:c.426-21G=	XP_006721011.1:n.426-21G=
XM_006720947.4:c.696-21G=	XP_006721010.1:n.696-21G=
XM_006720948.4:c.426-21G=	XP_006721011.1:n.426-21G=
NM_024589.3:c.696-42G= MANE Select	NP_078865.1:n.696-42G=
NR_046480.2:n.703-42G=