Canonical Allele Identifier: CA277136579

Gene: ROGDI

Linked Data

• dbSNP Id: rs771711821
• gnomAD v2: 16-4848301-GCTCTT-G
• gnomAD v3: 16-4798300-GCTCTT-G
• gnomAD v4: 16-4798300-GCTCTT-G
• MyVariant Identifiers: chr16:g.4848302_4848306del (hg19) ; chr16:g.4798301_4798305del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4798304_4798308del , CM000678.2:g.4798304_4798308del	GRCh38
NC_000016.9:g.4848305_4848309del , CM000678.1:g.4848305_4848309del	GRCh37
NC_000016.8:g.4788306_4788310del	NCBI36
NG_032174.1:g.9646_9650del , LRG_455:g.9646_9650del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.532-121_532-117del MANE Select	ENSP00000322832.6:n.532-121_532-117del
ENST00000322048.11:c.532-121_532-117del	ENSP00000322832.5:n.532-121_532-117del
ENST00000586153.1:c.178-121_178-117del	ENSP00000464699.1:n.178-121_178-117del
ENST00000586336.5:n.631-121_631-117del
ENST00000586504.5:c.312-121_312-117del
ENST00000587377.5:c.545-121_545-117del	ENSP00000468343.1:n.545-121_545-117del
ENST00000587711.5:c.217-121_217-117del	ENSP00000467459.1:n.217-121_217-117del
ENST00000587843.5:c.*270-121_*270-117del	ENSP00000465970.1:n.*270-121_*270-117del
ENST00000588201.5:c.*523-121_*523-117del	ENSP00000466529.1:n.*523-121_*523-117del
ENST00000589543.5:n.489-121_489-117del
ENST00000591292.5:n.1861-121_1861-117del
ENST00000591392.5:c.460-121_460-117del	ENSP00000467509.1:n.460-121_460-117del
ENST00000592019.1:c.77-490_77-486del
NM_024589.2:c.532-121_532-117del , LRG_455t1:c.532-121_532-117del	NP_078865.1:n.532-121_532-117del
NR_046480.1:n.856-121_856-117del
XM_006720947.2:c.532-121_532-117del	XP_006721010.1:n.532-121_532-117del
XM_006720948.2:c.262-121_262-117del	XP_006721011.1:n.262-121_262-117del
XM_006720947.4:c.532-121_532-117del	XP_006721010.1:n.532-121_532-117del
XM_006720948.4:c.262-121_262-117del	XP_006721011.1:n.262-121_262-117del
NM_024589.3:c.532-121_532-117del MANE Select	NP_078865.1:n.532-121_532-117del
NR_046480.2:n.539-121_539-117del