Canonical Allele Identifier: CA2575900149

Gene: ROGDI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4799802G>C , CM000678.2:g.4799802G>C	GRCh38
NC_000016.9:g.4849803G>C , CM000678.1:g.4849803G>C	GRCh37
NC_000016.8:g.4789804G>C	NCBI36
NG_032174.1:g.8149C>G , LRG_455:g.8149C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.337-21C>G MANE Select	ENSP00000322832.6:n.337-21C>G
ENST00000322048.11:c.337-21C>G	ENSP00000322832.5:n.337-21C>G
ENST00000585653.1:n.469-21C>G
ENST00000586153.1:c.82-21C>G	ENSP00000464699.1:n.82-21C>G
ENST00000586336.5:n.436-21C>G
ENST00000586504.5:c.117-21C>G
ENST00000587377.5:c.337-21C>G	ENSP00000468343.1:n.337-21C>G
ENST00000587711.5:c.118-1135C>G	ENSP00000467459.1:n.118-1135C>G
ENST00000587843.5:c.*75-21C>G	ENSP00000465970.1:n.*75-21C>G
ENST00000588201.5:c.*194-21C>G	ENSP00000466529.1:n.*194-21C>G
ENST00000589543.5:n.294-21C>G
ENST00000591292.5:n.1666-21C>G
ENST00000591392.5:c.265-21C>G	ENSP00000467509.1:n.265-21C>G
ENST00000592019.1:c.56-21C>G
NM_024589.2:c.337-21C>G , LRG_455t1:c.337-21C>G	NP_078865.1:n.337-21C>G
NR_046480.1:n.661-21C>G
XM_006720947.2:c.337-21C>G	XP_006721010.1:n.337-21C>G
XM_006720948.2:c.67-21C>G	XP_006721011.1:n.67-21C>G
XM_006720947.4:c.337-21C>G	XP_006721010.1:n.337-21C>G
XM_006720948.4:c.67-21C>G	XP_006721011.1:n.67-21C>G
NM_024589.3:c.337-21C>G MANE Select	NP_078865.1:n.337-21C>G
NR_046480.2:n.344-21C>G