Canonical Allele Identifier: CA2631551333

Gene: ROGDI

Linked Data

• gnomAD v4: 16-4798335-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4798335C>G , CM000678.2:g.4798335C>G	GRCh38
NC_000016.9:g.4848336C>G , CM000678.1:g.4848336C>G	GRCh37
NC_000016.8:g.4788337C>G	NCBI36
NG_032174.1:g.9616G>C , LRG_455:g.9616G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.532-151G>C MANE Select	ENSP00000322832.6:n.532-151G>C
ENST00000322048.11:c.532-151G>C	ENSP00000322832.5:n.532-151G>C
ENST00000586153.1:c.178-151G>C	ENSP00000464699.1:n.178-151G>C
ENST00000586336.5:n.631-151G>C
ENST00000586504.5:c.312-151G>C
ENST00000587377.5:c.545-151G>C	ENSP00000468343.1:n.545-151G>C
ENST00000587711.5:c.217-151G>C	ENSP00000467459.1:n.217-151G>C
ENST00000587843.5:c.*270-151G>C	ENSP00000465970.1:n.*270-151G>C
ENST00000588201.5:c.*523-151G>C	ENSP00000466529.1:n.*523-151G>C
ENST00000589543.5:n.489-151G>C
ENST00000591292.5:n.1861-151G>C
ENST00000591392.5:c.460-151G>C	ENSP00000467509.1:n.460-151G>C
ENST00000592019.1:c.77-520G>C
NM_024589.2:c.532-151G>C , LRG_455t1:c.532-151G>C	NP_078865.1:n.532-151G>C
NR_046480.1:n.856-151G>C
XM_006720947.2:c.532-151G>C	XP_006721010.1:n.532-151G>C
XM_006720948.2:c.262-151G>C	XP_006721011.1:n.262-151G>C
XM_006720947.4:c.532-151G>C	XP_006721010.1:n.532-151G>C
XM_006720948.4:c.262-151G>C	XP_006721011.1:n.262-151G>C
NM_024589.3:c.532-151G>C MANE Select	NP_078865.1:n.532-151G>C
NR_046480.2:n.539-151G>C