Canonical Allele Identifier: CA2203529134

Gene: ROGDI

Linked Data

• dbSNP Id: rs2082675400
• gnomAD v4: 16-4798059-GTC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4798060_4798061del , CM000678.2:g.4798060_4798061del	GRCh38
NC_000016.9:g.4848061_4848062del , CM000678.1:g.4848061_4848062del	GRCh37
NC_000016.8:g.4788062_4788063del	NCBI36
NG_032174.1:g.9890_9891del , LRG_455:g.9890_9891del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.645+10_645+11del MANE Select	ENSP00000322832.6:n.645+10_645+11del
ENST00000322048.11:c.645+10_645+11del	ENSP00000322832.5:n.645+10_645+11del
ENST00000586153.1:c.291+10_291+11del	ENSP00000464699.1:n.291+10_291+11del
ENST00000586336.5:n.744+10_744+11del
ENST00000586504.5:c.425+10_425+11del
ENST00000587377.5:c.658+10_658+11del	ENSP00000468343.1:n.658+10_658+11del
ENST00000587711.5:c.330+10_330+11del	ENSP00000467459.1:n.330+10_330+11del
ENST00000587843.5:c.*383+10_*383+11del	ENSP00000465970.1:n.*383+10_*383+11del
ENST00000588201.5:c.*636+10_*636+11del	ENSP00000466529.1:n.*636+10_*636+11del
ENST00000589543.5:n.602+10_602+11del
ENST00000591292.5:n.1974+10_1974+11del
ENST00000591392.5:c.573+10_573+11del	ENSP00000467509.1:n.573+10_573+11del
ENST00000592019.1:c.77-246_77-245del
NM_024589.2:c.645+10_645+11del , LRG_455t1:c.645+10_645+11del	NP_078865.1:n.645+10_645+11del
NR_046480.1:n.969+10_969+11del
XM_006720947.2:c.645+10_645+11del	XP_006721010.1:n.645+10_645+11del
XM_006720948.2:c.375+10_375+11del	XP_006721011.1:n.375+10_375+11del
XM_006720947.4:c.645+10_645+11del	XP_006721010.1:n.645+10_645+11del
XM_006720948.4:c.375+10_375+11del	XP_006721011.1:n.375+10_375+11del
NM_024589.3:c.645+10_645+11del MANE Select	NP_078865.1:n.645+10_645+11del
NR_046480.2:n.652+10_652+11del