Canonical Allele Identifier: CA277136714

Gene: ROGDI

Linked Data

• dbSNP Id: rs1033208911
• gnomAD v4: 16-4798447-T-C
• MyVariant Identifiers: chr16:g.4848448T>C (hg19) ; chr16:g.4798447T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4798447T>C , CM000678.2:g.4798447T>C	GRCh38
NC_000016.9:g.4848448T>C , CM000678.1:g.4848448T>C	GRCh37
NC_000016.8:g.4788449T>C	NCBI36
NG_032174.1:g.9504A>G , LRG_455:g.9504A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.531+122A>G MANE Select	ENSP00000322832.6:n.531+122A>G
ENST00000322048.11:c.531+122A>G	ENSP00000322832.5:n.531+122A>G
ENST00000586153.1:c.178-263A>G	ENSP00000464699.1:n.178-263A>G
ENST00000586336.5:n.630+122A>G
ENST00000586504.5:c.311+122A>G
ENST00000587377.5:c.544+122A>G	ENSP00000468343.1:n.544+122A>G
ENST00000587711.5:c.216+122A>G	ENSP00000467459.1:n.216+122A>G
ENST00000587843.5:c.*269+122A>G	ENSP00000465970.1:n.*269+122A>G
ENST00000588201.5:c.*522+122A>G	ENSP00000466529.1:n.*522+122A>G
ENST00000589543.5:n.488+122A>G
ENST00000591292.5:n.1860+122A>G
ENST00000591392.5:c.459+122A>G	ENSP00000467509.1:n.459+122A>G
ENST00000592019.1:c.77-632A>G
NM_024589.2:c.531+122A>G , LRG_455t1:c.531+122A>G	NP_078865.1:n.531+122A>G
NR_046480.1:n.855+122A>G
XM_006720947.2:c.531+122A>G	XP_006721010.1:n.531+122A>G
XM_006720948.2:c.261+122A>G	XP_006721011.1:n.261+122A>G
XM_006720947.4:c.531+122A>G	XP_006721010.1:n.531+122A>G
XM_006720948.4:c.261+122A>G	XP_006721011.1:n.261+122A>G
NM_024589.3:c.531+122A>G MANE Select	NP_078865.1:n.531+122A>G
NR_046480.2:n.538+122A>G