Canonical Allele Identifier: CA7882587

Gene: ROGDI

Linked Data

• dbSNP Id: rs754215549
• ExAC: 16:4848026 GGC / G
• gnomAD v2: 16-4848026-GGC-G
• gnomAD v4: 16-4798025-GGC-G
• MyVariant Identifiers: chr16:g.4848027_4848028del (hg19) ; chr16:g.4798026_4798027del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4798027_4798028del , CM000678.2:g.4798027_4798028del	GRCh38
NC_000016.9:g.4848028_4848029del , CM000678.1:g.4848028_4848029del	GRCh37
NC_000016.8:g.4788029_4788030del	NCBI36
NG_032174.1:g.9924_9925del , LRG_455:g.9924_9925del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.646-40_646-39del MANE Select	ENSP00000322832.6:n.646-40_646-39del
ENST00000322048.11:c.646-40_646-39del	ENSP00000322832.5:n.646-40_646-39del
ENST00000586153.1:c.292-40_292-39del	ENSP00000464699.1:n.292-40_292-39del
ENST00000586336.5:n.745-40_745-39del
ENST00000586504.5:c.425+44_425+45del
ENST00000587377.5:c.659-40_659-39del	ENSP00000468343.1:n.659-40_659-39del
ENST00000587711.5:c.331-40_331-39del	ENSP00000467459.1:n.331-40_331-39del
ENST00000587843.5:c.*384-40_*384-39del	ENSP00000465970.1:n.*384-40_*384-39del
ENST00000588201.5:c.*637-40_*637-39del	ENSP00000466529.1:n.*637-40_*637-39del
ENST00000589543.5:n.603-40_603-39del
ENST00000591292.5:n.1975-40_1975-39del
ENST00000591392.5:c.574-40_574-39del	ENSP00000467509.1:n.574-40_574-39del
ENST00000592019.1:c.77-212_77-211del
NM_024589.2:c.646-40_646-39del , LRG_455t1:c.646-40_646-39del	NP_078865.1:n.646-40_646-39del
NR_046480.1:n.970-40_970-39del
XM_006720947.2:c.646-40_646-39del	XP_006721010.1:n.646-40_646-39del
XM_006720948.2:c.376-40_376-39del	XP_006721011.1:n.376-40_376-39del
XM_006720947.4:c.646-40_646-39del	XP_006721010.1:n.646-40_646-39del
XM_006720948.4:c.376-40_376-39del	XP_006721011.1:n.376-40_376-39del
NM_024589.3:c.646-40_646-39del MANE Select	NP_078865.1:n.646-40_646-39del
NR_046480.2:n.653-40_653-39del