Canonical Allele Identifier: CA277136655

Gene: ROGDI

Linked Data

• dbSNP Id: rs886519482
• gnomAD v3: 16-4798386-A-C
• gnomAD v4: 16-4798386-A-C
• MyVariant Identifiers: chr16:g.4848387A>C (hg19) ; chr16:g.4798386A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4798386A>C , CM000678.2:g.4798386A>C	GRCh38
NC_000016.9:g.4848387A>C , CM000678.1:g.4848387A>C	GRCh37
NC_000016.8:g.4788388A>C	NCBI36
NG_032174.1:g.9565T>G , LRG_455:g.9565T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.531+183T>G MANE Select	ENSP00000322832.6:n.531+183T>G
ENST00000322048.11:c.531+183T>G	ENSP00000322832.5:n.531+183T>G
ENST00000586153.1:c.178-202T>G	ENSP00000464699.1:n.178-202T>G
ENST00000586336.5:n.630+183T>G
ENST00000586504.5:c.311+183T>G
ENST00000587377.5:c.544+183T>G	ENSP00000468343.1:n.544+183T>G
ENST00000587711.5:c.216+183T>G	ENSP00000467459.1:n.216+183T>G
ENST00000587843.5:c.*269+183T>G	ENSP00000465970.1:n.*269+183T>G
ENST00000588201.5:c.*522+183T>G	ENSP00000466529.1:n.*522+183T>G
ENST00000589543.5:n.488+183T>G
ENST00000591292.5:n.1860+183T>G
ENST00000591392.5:c.459+183T>G	ENSP00000467509.1:n.459+183T>G
ENST00000592019.1:c.77-571T>G
NM_024589.2:c.531+183T>G , LRG_455t1:c.531+183T>G	NP_078865.1:n.531+183T>G
NR_046480.1:n.855+183T>G
XM_006720947.2:c.531+183T>G	XP_006721010.1:n.531+183T>G
XM_006720948.2:c.261+183T>G	XP_006721011.1:n.261+183T>G
XM_006720947.4:c.531+183T>G	XP_006721010.1:n.531+183T>G
XM_006720948.4:c.261+183T>G	XP_006721011.1:n.261+183T>G
NM_024589.3:c.531+183T>G MANE Select	NP_078865.1:n.531+183T>G
NR_046480.2:n.538+183T>G