Canonical Allele Identifier: CA7882584

Gene: ROGDI

Linked Data

• dbSNP Id: rs764457838
• ExAC: 16:4848019 C / CT
• gnomAD v2: 16-4848019-C-CT
• gnomAD v3: 16-4798018-C-CT
• gnomAD v4: 16-4798018-C-CT
• MyVariant Identifiers: chr16:g.4848019_4848020insT (hg19) ; chr16:g.4798018_4798019insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4798020dup , CM000678.2:g.4798020dup	GRCh38
NC_000016.9:g.4848021dup , CM000678.1:g.4848021dup	GRCh37
NC_000016.8:g.4788022dup	NCBI36
NG_032174.1:g.9932dup , LRG_455:g.9932dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.646-32dup MANE Select	ENSP00000322832.6:n.646-32dup
ENST00000322048.11:c.646-32dup	ENSP00000322832.5:n.646-32dup
ENST00000586153.1:c.292-32dup	ENSP00000464699.1:n.292-32dup
ENST00000586336.5:n.745-32dup
ENST00000586504.5:c.425+52dup
ENST00000587377.5:c.659-32dup	ENSP00000468343.1:n.659-32dup
ENST00000587711.5:c.331-32dup	ENSP00000467459.1:n.331-32dup
ENST00000587843.5:c.*384-32dup	ENSP00000465970.1:n.*384-32dup
ENST00000588201.5:c.*637-32dup	ENSP00000466529.1:n.*637-32dup
ENST00000589543.5:n.603-32dup
ENST00000591292.5:n.1975-32dup
ENST00000591392.5:c.574-32dup	ENSP00000467509.1:n.574-32dup
ENST00000592019.1:c.77-204dup
NM_024589.2:c.646-32dup , LRG_455t1:c.646-32dup	NP_078865.1:n.646-32dup
NR_046480.1:n.970-32dup
XM_006720947.2:c.646-32dup	XP_006721010.1:n.646-32dup
XM_006720948.2:c.376-32dup	XP_006721011.1:n.376-32dup
XM_006720947.4:c.646-32dup	XP_006721010.1:n.646-32dup
XM_006720948.4:c.376-32dup	XP_006721011.1:n.376-32dup
NM_024589.3:c.646-32dup MANE Select	NP_078865.1:n.646-32dup
NR_046480.2:n.653-32dup