Canonical Allele Identifier: CA7882638

Gene: ROGDI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4798157C>T , CM000678.2:g.4798157C>T	GRCh38
NC_000016.9:g.4848158C>T , CM000678.1:g.4848158C>T	GRCh37
NC_000016.8:g.4788159C>T	NCBI36
NG_032174.1:g.9794G>A , LRG_455:g.9794G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_024589.3:c.559G>A MANE Select	NP_078865.1:p.Asp187Asn
ENST00000322048.12:c.559G>A MANE Select	ENSP00000322832.6:p.Asp187Asn
NM_024589.2:c.559G>A , LRG_455t1:c.559G>A	NP_078865.1:p.Asp187Asn
NR_046480.1:n.883G>A
NR_046480.2:n.566G>A
ENST00000322048.11:c.559G>A	ENSP00000322832.5:p.Asp187Asn
ENST00000586153.1:c.205G>A	ENSP00000464699.1:p.Asp69Asn
ENST00000586336.5:n.658G>A
ENST00000586504.5:c.339G>A
ENST00000587377.5:c.572G>A	ENSP00000468343.1:p.Arg191Gln
ENST00000587711.5:c.244G>A	ENSP00000467459.1:p.Asp82Asn
ENST00000587843.5:c.*297G>A	ENSP00000465970.1:n.*297G>A
ENST00000588201.5:c.*550G>A	ENSP00000466529.1:n.*550G>A
ENST00000589543.5:n.516G>A
ENST00000591292.5:n.1888G>A
ENST00000591392.5:c.487G>A	ENSP00000467509.1:p.Asp163Asn
ENST00000592019.1:c.77-342G>A
XM_006720947.2:c.559G>A	XP_006721010.1:p.Asp187Asn
XM_006720947.4:c.559G>A	XP_006721010.1:p.Asp187Asn
XM_006720948.2:c.289G>A	XP_006721011.1:p.Asp97Asn
XM_006720948.4:c.289G>A	XP_006721011.1:p.Asp97Asn