Canonical Allele Identifier: CA2203528993

Gene: ROGDI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4797894G= , CM000678.2:g.4797894G=	GRCh38
NC_000016.9:g.4847895G= , CM000678.1:g.4847895G=	GRCh37
NC_000016.8:g.4787896G=	NCBI36
NG_032174.1:g.10057C= , LRG_455:g.10057C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.695+44C= MANE Select	ENSP00000322832.6:n.695+44C=
ENST00000322048.11:c.695+44C=	ENSP00000322832.5:n.695+44C=
ENST00000586153.1:c.341+44C=	ENSP00000464699.1:n.341+44C=
ENST00000586336.5:n.794+44C=
ENST00000586504.5:c.426-54C=
ENST00000587377.5:c.*15+44C=	ENSP00000468343.1:n.*15+44C=
ENST00000587711.5:c.380+44C=	ENSP00000467459.1:n.380+44C=
ENST00000587843.5:c.*433+44C=	ENSP00000465970.1:n.*433+44C=
ENST00000588201.5:c.*686+44C=	ENSP00000466529.1:n.*686+44C=
ENST00000589543.5:n.652+44C=
ENST00000591292.5:n.2024+44C=
ENST00000591392.5:c.623+44C=	ENSP00000467509.1:n.623+44C=
ENST00000592019.1:c.77-79C=
NM_024589.2:c.695+44C= , LRG_455t1:c.695+44C=	NP_078865.1:n.695+44C=
NR_046480.1:n.1019+44C=
XM_006720947.2:c.696-33C=	XP_006721010.1:n.696-33C=
XM_006720948.2:c.426-33C=	XP_006721011.1:n.426-33C=
XM_006720947.4:c.696-33C=	XP_006721010.1:n.696-33C=
XM_006720948.4:c.426-33C=	XP_006721011.1:n.426-33C=
NM_024589.3:c.695+44C= MANE Select	NP_078865.1:n.695+44C=
NR_046480.2:n.702+44C=