Canonical Allele Identifier: CA394653204

Gene: ROGDI

Linked Data

• MyVariant Identifiers: chr16:g.4849700G>C (hg19) ; chr16:g.4799699G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4799699G>C , CM000678.2:g.4799699G>C	GRCh38
NC_000016.9:g.4849700G>C , CM000678.1:g.4849700G>C	GRCh37
NC_000016.8:g.4789701G>C	NCBI36
NG_032174.1:g.8252C>G , LRG_455:g.8252C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.419C>G MANE Select	ENSP00000322832.6:p.Ala140Gly
ENST00000322048.11:c.419C>G	ENSP00000322832.5:p.Ala140Gly
ENST00000585653.1:n.551C>G
ENST00000586153.1:c.164C>G	ENSP00000464699.1:p.Ala55Gly
ENST00000586336.5:n.518C>G
ENST00000586504.5:c.199C>G
ENST00000587377.5:c.419C>G	ENSP00000468343.1:p.Ala140Gly
ENST00000587711.5:c.118-1032C>G	ENSP00000467459.1:n.118-1032C>G
ENST00000587843.5:c.*157C>G	ENSP00000465970.1:n.*157C>G
ENST00000588201.5:c.*276C>G	ENSP00000466529.1:n.*276C>G
ENST00000589543.5:n.376C>G
ENST00000591292.5:n.1748C>G
ENST00000591392.5:c.347C>G	ENSP00000467509.1:p.Ala116Gly
ENST00000592019.1:c.76+62C>G
NM_024589.2:c.419C>G , LRG_455t1:c.419C>G	NP_078865.1:p.Ala140Gly
NR_046480.1:n.743C>G
XM_006720947.2:c.419C>G	XP_006721010.1:p.Ala140Gly
XM_006720948.2:c.149C>G	XP_006721011.1:p.Ala50Gly
XM_006720947.4:c.419C>G	XP_006721010.1:p.Ala140Gly
XM_006720948.4:c.149C>G	XP_006721011.1:p.Ala50Gly
NM_024589.3:c.419C>G MANE Select	NP_078865.1:p.Ala140Gly
NR_046480.2:n.426C>G