Canonical Allele Identifier: CA2203529323

Gene: ROGDI

Linked Data

• dbSNP Id: rs1596275278

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4798317G>C , CM000678.2:g.4798317G>C	GRCh38
NC_000016.9:g.4848318G>C , CM000678.1:g.4848318G>C	GRCh37
NC_000016.8:g.4788319G>C	NCBI36
NG_032174.1:g.9634C>G , LRG_455:g.9634C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.532-133C>G MANE Select	ENSP00000322832.6:n.532-133C>G
ENST00000322048.11:c.532-133C>G	ENSP00000322832.5:n.532-133C>G
ENST00000586153.1:c.178-133C>G	ENSP00000464699.1:n.178-133C>G
ENST00000586336.5:n.631-133C>G
ENST00000586504.5:c.312-133C>G
ENST00000587377.5:c.545-133C>G	ENSP00000468343.1:n.545-133C>G
ENST00000587711.5:c.217-133C>G	ENSP00000467459.1:n.217-133C>G
ENST00000587843.5:c.*270-133C>G	ENSP00000465970.1:n.*270-133C>G
ENST00000588201.5:c.*523-133C>G	ENSP00000466529.1:n.*523-133C>G
ENST00000589543.5:n.489-133C>G
ENST00000591292.5:n.1861-133C>G
ENST00000591392.5:c.460-133C>G	ENSP00000467509.1:n.460-133C>G
ENST00000592019.1:c.77-502C>G
NM_024589.2:c.532-133C>G , LRG_455t1:c.532-133C>G	NP_078865.1:n.532-133C>G
NR_046480.1:n.856-133C>G
XM_006720947.2:c.532-133C>G	XP_006721010.1:n.532-133C>G
XM_006720948.2:c.262-133C>G	XP_006721011.1:n.262-133C>G
XM_006720947.4:c.532-133C>G	XP_006721010.1:n.532-133C>G
XM_006720948.4:c.262-133C>G	XP_006721011.1:n.262-133C>G
NM_024589.3:c.532-133C>G MANE Select	NP_078865.1:n.532-133C>G
NR_046480.2:n.539-133C>G