Canonical Allele Identifier: CA2631551227

Gene: ROGDI

Linked Data

• gnomAD v4: 16-4798293-CAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4798297_4798298del , CM000678.2:g.4798297_4798298del	GRCh38
NC_000016.9:g.4848298_4848299del , CM000678.1:g.4848298_4848299del	GRCh37
NC_000016.8:g.4788299_4788300del	NCBI36
NG_032174.1:g.9656_9657del , LRG_455:g.9656_9657del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.532-111_532-110del MANE Select	ENSP00000322832.6:n.532-111_532-110del
ENST00000322048.11:c.532-111_532-110del	ENSP00000322832.5:n.532-111_532-110del
ENST00000586153.1:c.178-111_178-110del	ENSP00000464699.1:n.178-111_178-110del
ENST00000586336.5:n.631-111_631-110del
ENST00000586504.5:c.312-111_312-110del
ENST00000587377.5:c.545-111_545-110del	ENSP00000468343.1:n.545-111_545-110del
ENST00000587711.5:c.217-111_217-110del	ENSP00000467459.1:n.217-111_217-110del
ENST00000587843.5:c.*270-111_*270-110del	ENSP00000465970.1:n.*270-111_*270-110del
ENST00000588201.5:c.*523-111_*523-110del	ENSP00000466529.1:n.*523-111_*523-110del
ENST00000589543.5:n.489-111_489-110del
ENST00000591292.5:n.1861-111_1861-110del
ENST00000591392.5:c.460-111_460-110del	ENSP00000467509.1:n.460-111_460-110del
ENST00000592019.1:c.77-480_77-479del
NM_024589.2:c.532-111_532-110del , LRG_455t1:c.532-111_532-110del	NP_078865.1:n.532-111_532-110del
NR_046480.1:n.856-111_856-110del
XM_006720947.2:c.532-111_532-110del	XP_006721010.1:n.532-111_532-110del
XM_006720948.2:c.262-111_262-110del	XP_006721011.1:n.262-111_262-110del
XM_006720947.4:c.532-111_532-110del	XP_006721010.1:n.532-111_532-110del
XM_006720948.4:c.262-111_262-110del	XP_006721011.1:n.262-111_262-110del
NM_024589.3:c.532-111_532-110del MANE Select	NP_078865.1:n.532-111_532-110del
NR_046480.2:n.539-111_539-110del