Canonical Allele Identifier: CA2631553085

Gene: ROGDI

Linked Data

• gnomAD v4: 16-4799660-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4799660A>G , CM000678.2:g.4799660A>G	GRCh38
NC_000016.9:g.4849661A>G , CM000678.1:g.4849661A>G	GRCh37
NC_000016.8:g.4789662A>G	NCBI36
NG_032174.1:g.8291T>C , LRG_455:g.8291T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.432+26T>C MANE Select	ENSP00000322832.6:n.432+26T>C
ENST00000322048.11:c.432+26T>C	ENSP00000322832.5:n.432+26T>C
ENST00000585653.1:n.564+26T>C
ENST00000586153.1:c.177+26T>C	ENSP00000464699.1:n.177+26T>C
ENST00000586336.5:n.531+26T>C
ENST00000586504.5:c.212+26T>C
ENST00000587377.5:c.423+35T>C	ENSP00000468343.1:n.423+35T>C
ENST00000587711.5:c.118-993T>C	ENSP00000467459.1:n.118-993T>C
ENST00000587843.5:c.*170+26T>C	ENSP00000465970.1:n.*170+26T>C
ENST00000588201.5:c.*289+26T>C	ENSP00000466529.1:n.*289+26T>C
ENST00000589543.5:n.389+26T>C
ENST00000591292.5:n.1761+26T>C
ENST00000591392.5:c.360+26T>C	ENSP00000467509.1:n.360+26T>C
ENST00000592019.1:c.76+101T>C
NM_024589.2:c.432+26T>C , LRG_455t1:c.432+26T>C	NP_078865.1:n.432+26T>C
NR_046480.1:n.756+26T>C
XM_006720947.2:c.432+26T>C	XP_006721010.1:n.432+26T>C
XM_006720948.2:c.162+26T>C	XP_006721011.1:n.162+26T>C
XM_006720947.4:c.432+26T>C	XP_006721010.1:n.432+26T>C
XM_006720948.4:c.162+26T>C	XP_006721011.1:n.162+26T>C
NM_024589.3:c.432+26T>C MANE Select	NP_078865.1:n.432+26T>C
NR_046480.2:n.439+26T>C