Canonical Allele Identifier: CA2631549999

Gene: ROGDI

Linked Data

• gnomAD v4: 16-4797870-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4797870G>C , CM000678.2:g.4797870G>C	GRCh38
NC_000016.9:g.4847871G>C , CM000678.1:g.4847871G>C	GRCh37
NC_000016.8:g.4787872G>C	NCBI36
NG_032174.1:g.10081C>G , LRG_455:g.10081C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.696-30C>G MANE Select	ENSP00000322832.6:n.696-30C>G
ENST00000322048.11:c.696-30C>G	ENSP00000322832.5:n.696-30C>G
ENST00000586153.1:c.342-34C>G	ENSP00000464699.1:n.342-34C>G
ENST00000586336.5:n.795-30C>G
ENST00000586504.5:c.426-30C>G
ENST00000587377.5:c.*16-30C>G	ENSP00000468343.1:n.*16-30C>G
ENST00000587711.5:c.381-30C>G	ENSP00000467459.1:n.381-30C>G
ENST00000587843.5:c.*434-30C>G	ENSP00000465970.1:n.*434-30C>G
ENST00000588201.5:c.*687-30C>G	ENSP00000466529.1:n.*687-30C>G
ENST00000589543.5:n.653-30C>G
ENST00000591292.5:n.2025-30C>G
ENST00000591392.5:c.624-30C>G	ENSP00000467509.1:n.624-30C>G
ENST00000592019.1:c.77-55C>G
NM_024589.2:c.696-30C>G , LRG_455t1:c.696-30C>G	NP_078865.1:n.696-30C>G
NR_046480.1:n.1020-30C>G
XM_006720947.2:c.696-9C>G	XP_006721010.1:n.696-9C>G
XM_006720948.2:c.426-9C>G	XP_006721011.1:n.426-9C>G
XM_006720947.4:c.696-9C>G	XP_006721010.1:n.696-9C>G
XM_006720948.4:c.426-9C>G	XP_006721011.1:n.426-9C>G
NM_024589.3:c.696-30C>G MANE Select	NP_078865.1:n.696-30C>G
NR_046480.2:n.703-30C>G