Canonical Allele Identifier: CA2631553270

Gene: ROGDI

Linked Data

• gnomAD v4: 16-4799807-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4799807G>C , CM000678.2:g.4799807G>C	GRCh38
NC_000016.9:g.4849808G>C , CM000678.1:g.4849808G>C	GRCh37
NC_000016.8:g.4789809G>C	NCBI36
NG_032174.1:g.8144C>G , LRG_455:g.8144C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.337-26C>G MANE Select	ENSP00000322832.6:n.337-26C>G
ENST00000322048.11:c.337-26C>G	ENSP00000322832.5:n.337-26C>G
ENST00000585653.1:n.469-26C>G
ENST00000586153.1:c.82-26C>G	ENSP00000464699.1:n.82-26C>G
ENST00000586336.5:n.436-26C>G
ENST00000586504.5:c.117-26C>G
ENST00000587377.5:c.337-26C>G	ENSP00000468343.1:n.337-26C>G
ENST00000587711.5:c.118-1140C>G	ENSP00000467459.1:n.118-1140C>G
ENST00000587843.5:c.*75-26C>G	ENSP00000465970.1:n.*75-26C>G
ENST00000588201.5:c.*194-26C>G	ENSP00000466529.1:n.*194-26C>G
ENST00000589543.5:n.294-26C>G
ENST00000591292.5:n.1666-26C>G
ENST00000591392.5:c.265-26C>G	ENSP00000467509.1:n.265-26C>G
ENST00000592019.1:c.56-26C>G
NM_024589.2:c.337-26C>G , LRG_455t1:c.337-26C>G	NP_078865.1:n.337-26C>G
NR_046480.1:n.661-26C>G
XM_006720947.2:c.337-26C>G	XP_006721010.1:n.337-26C>G
XM_006720948.2:c.67-26C>G	XP_006721011.1:n.67-26C>G
XM_006720947.4:c.337-26C>G	XP_006721010.1:n.337-26C>G
XM_006720948.4:c.67-26C>G	XP_006721011.1:n.67-26C>G
NM_024589.3:c.337-26C>G MANE Select	NP_078865.1:n.337-26C>G
NR_046480.2:n.344-26C>G