Canonical Allele Identifier: CA493320324

Gene: ROGDI

Linked Data

• MyVariant Identifiers: chr16:g.4849729C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4799728C>G , CM000678.2:g.4799728C>G	GRCh38
NC_000016.9:g.4849729C>G , CM000678.1:g.4849729C>G	GRCh37
NC_000016.8:g.4789730C>G	NCBI36
NG_032174.1:g.8223G>C , LRG_455:g.8223G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.390G>C MANE Select	ENSP00000322832.6:p.Arg130=
ENST00000322048.11:c.390G>C	ENSP00000322832.5:p.Arg130=
ENST00000585653.1:n.522G>C
ENST00000586153.1:c.135G>C	ENSP00000464699.1:p.Arg45=
ENST00000586336.5:n.489G>C
ENST00000586504.5:c.170G>C
ENST00000587377.5:c.390G>C	ENSP00000468343.1:p.Arg130=
ENST00000587711.5:c.118-1061G>C	ENSP00000467459.1:n.118-1061G>C
ENST00000587843.5:c.*128G>C	ENSP00000465970.1:n.*128G>C
ENST00000588201.5:c.*247G>C	ENSP00000466529.1:n.*247G>C
ENST00000589543.5:n.347G>C
ENST00000591292.5:n.1719G>C
ENST00000591392.5:c.318G>C	ENSP00000467509.1:p.Arg106=
ENST00000592019.1:c.76+33G>C
NM_024589.2:c.390G>C , LRG_455t1:c.390G>C	NP_078865.1:p.Arg130=
NR_046480.1:n.714G>C
XM_006720947.2:c.390G>C	XP_006721010.1:p.Arg130=
XM_006720948.2:c.120G>C	XP_006721011.1:p.Arg40=
XM_006720947.4:c.390G>C	XP_006721010.1:p.Arg130=
XM_006720948.4:c.120G>C	XP_006721011.1:p.Arg40=
NM_024589.3:c.390G>C MANE Select	NP_078865.1:p.Arg130=
NR_046480.2:n.397G>C