Canonical Allele Identifier: CA2805667691

Gene: ROGDI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4797911_4797914del , CM000678.2:g.4797911_4797914del	GRCh38
NC_000016.9:g.4847912_4847915del , CM000678.1:g.4847912_4847915del	GRCh37
NC_000016.8:g.4787913_4787916del	NCBI36
NG_032174.1:g.10037_10040del , LRG_455:g.10037_10040del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.695+24_695+27del MANE Select	ENSP00000322832.6:n.695+24_695+27del
ENST00000322048.11:c.695+24_695+27del	ENSP00000322832.5:n.695+24_695+27del
ENST00000586153.1:c.341+24_341+27del	ENSP00000464699.1:n.341+24_341+27del
ENST00000586336.5:n.794+24_794+27del
ENST00000586504.5:c.426-74_426-71del
ENST00000587377.5:c.*15+24_*15+27del	ENSP00000468343.1:n.*15+24_*15+27del
ENST00000587711.5:c.380+24_380+27del	ENSP00000467459.1:n.380+24_380+27del
ENST00000587843.5:c.*433+24_*433+27del	ENSP00000465970.1:n.*433+24_*433+27del
ENST00000588201.5:c.*686+24_*686+27del	ENSP00000466529.1:n.*686+24_*686+27del
ENST00000589543.5:n.652+24_652+27del
ENST00000591292.5:n.2024+24_2024+27del
ENST00000591392.5:c.623+24_623+27del	ENSP00000467509.1:n.623+24_623+27del
ENST00000592019.1:c.77-99_77-96del
NM_024589.2:c.695+24_695+27del , LRG_455t1:c.695+24_695+27del	NP_078865.1:n.695+24_695+27del
NR_046480.1:n.1019+24_1019+27del
XM_006720947.2:c.695+24_695+27del	XP_006721010.1:n.695+24_695+27del
XM_006720948.2:c.425+24_425+27del	XP_006721011.1:n.425+24_425+27del
XM_006720947.4:c.695+24_695+27del	XP_006721010.1:n.695+24_695+27del
XM_006720948.4:c.425+24_425+27del	XP_006721011.1:n.425+24_425+27del
NM_024589.3:c.695+24_695+27del MANE Select	NP_078865.1:n.695+24_695+27del
NR_046480.2:n.702+24_702+27del