Canonical Allele Identifier: CA2203528995

Gene: ROGDI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4797896A= , CM000678.2:g.4797896A=	GRCh38
NC_000016.9:g.4847897A= , CM000678.1:g.4847897A=	GRCh37
NC_000016.8:g.4787898A=	NCBI36
NG_032174.1:g.10055T= , LRG_455:g.10055T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.695+42T= MANE Select	ENSP00000322832.6:n.695+42T=
ENST00000322048.11:c.695+42T=	ENSP00000322832.5:n.695+42T=
ENST00000586153.1:c.341+42T=	ENSP00000464699.1:n.341+42T=
ENST00000586336.5:n.794+42T=
ENST00000586504.5:c.426-56T=
ENST00000587377.5:c.*15+42T=	ENSP00000468343.1:n.*15+42T=
ENST00000587711.5:c.380+42T=	ENSP00000467459.1:n.380+42T=
ENST00000587843.5:c.*433+42T=	ENSP00000465970.1:n.*433+42T=
ENST00000588201.5:c.*686+42T=	ENSP00000466529.1:n.*686+42T=
ENST00000589543.5:n.652+42T=
ENST00000591292.5:n.2024+42T=
ENST00000591392.5:c.623+42T=	ENSP00000467509.1:n.623+42T=
ENST00000592019.1:c.77-81T=
NM_024589.2:c.695+42T= , LRG_455t1:c.695+42T=	NP_078865.1:n.695+42T=
NR_046480.1:n.1019+42T=
XM_006720947.2:c.696-35T=	XP_006721010.1:n.696-35T=
XM_006720948.2:c.426-35T=	XP_006721011.1:n.426-35T=
XM_006720947.4:c.696-35T=	XP_006721010.1:n.696-35T=
XM_006720948.4:c.426-35T=	XP_006721011.1:n.426-35T=
NM_024589.3:c.695+42T= MANE Select	NP_078865.1:n.695+42T=
NR_046480.2:n.702+42T=