Canonical Allele Identifier: CA2203529024

Gene: ROGDI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4797925C= , CM000678.2:g.4797925C=	GRCh38
NC_000016.9:g.4847926C= , CM000678.1:g.4847926C=	GRCh37
NC_000016.8:g.4787927C=	NCBI36
NG_032174.1:g.10026G= , LRG_455:g.10026G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.695+13G= MANE Select	ENSP00000322832.6:n.695+13G=
ENST00000322048.11:c.695+13G=	ENSP00000322832.5:n.695+13G=
ENST00000586153.1:c.341+13G=	ENSP00000464699.1:n.341+13G=
ENST00000586336.5:n.794+13G=
ENST00000586504.5:c.426-85G=
ENST00000587377.5:c.*15+13G=	ENSP00000468343.1:n.*15+13G=
ENST00000587711.5:c.380+13G=	ENSP00000467459.1:n.380+13G=
ENST00000587843.5:c.*433+13G=	ENSP00000465970.1:n.*433+13G=
ENST00000588201.5:c.*686+13G=	ENSP00000466529.1:n.*686+13G=
ENST00000589543.5:n.652+13G=
ENST00000591292.5:n.2024+13G=
ENST00000591392.5:c.623+13G=	ENSP00000467509.1:n.623+13G=
ENST00000592019.1:c.77-110G=
NM_024589.2:c.695+13G= , LRG_455t1:c.695+13G=	NP_078865.1:n.695+13G=
NR_046480.1:n.1019+13G=
XM_006720947.2:c.695+13G=	XP_006721010.1:n.695+13G=
XM_006720948.2:c.425+13G=	XP_006721011.1:n.425+13G=
XM_006720947.4:c.695+13G=	XP_006721010.1:n.695+13G=
XM_006720948.4:c.425+13G=	XP_006721011.1:n.425+13G=
NM_024589.3:c.695+13G= MANE Select	NP_078865.1:n.695+13G=
NR_046480.2:n.702+13G=