Canonical Allele Identifier: CA2805667698
Gene: ROGDI HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.4798229_4798230insACACA , CM000678.2:g.4798229_4798230insACACA GRCh38
NC_000016.9:g.4848230_4848231insACACA , CM000678.1:g.4848230_4848231insACACA GRCh37
NC_000016.8:g.4788231_4788232insACACA NCBI36
NG_032174.1:g.9723_9724insTGTTG , LRG_455:g.9723_9724insTGTTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000322048.12:c.532-44_532-43insTGTTG MANE Select ENSP00000322832.6:n.532-44_532-43insTGTTG
ENST00000322048.11:c.532-44_532-43insTGTTG ENSP00000322832.5:n.532-44_532-43insTGTTG
ENST00000586153.1:c.178-44_178-43insTGTTG ENSP00000464699.1:n.178-44_178-43insTGTTG
ENST00000586336.5:n.631-44_631-43insTGTTG
ENST00000586504.5:c.312-44_312-43insTGTTG
ENST00000587377.5:c.545-44_545-43insTGTTG ENSP00000468343.1:n.545-44_545-43insTGTTG
ENST00000587711.5:c.217-44_217-43insTGTTG ENSP00000467459.1:n.217-44_217-43insTGTTG
ENST00000587843.5:c.*270-44_*270-43insTGTTG ENSP00000465970.1:n.*270-44_*270-43insTGTTG
ENST00000588201.5:c.*523-44_*523-43insTGTTG ENSP00000466529.1:n.*523-44_*523-43insTGTTG
ENST00000589543.5:n.489-44_489-43insTGTTG
ENST00000591292.5:n.1861-44_1861-43insTGTTG
ENST00000591392.5:c.460-44_460-43insTGTTG ENSP00000467509.1:n.460-44_460-43insTGTTG
ENST00000592019.1:c.77-413_77-412insTGTTG
NM_024589.2:c.532-44_532-43insTGTTG , LRG_455t1:c.532-44_532-43insTGTTG NP_078865.1:n.532-44_532-43insTGTTG
NR_046480.1:n.856-44_856-43insTGTTG
XM_006720947.2:c.532-44_532-43insTGTTG XP_006721010.1:n.532-44_532-43insTGTTG
XM_006720948.2:c.262-44_262-43insTGTTG XP_006721011.1:n.262-44_262-43insTGTTG
XM_006720947.4:c.532-44_532-43insTGTTG XP_006721010.1:n.532-44_532-43insTGTTG
XM_006720948.4:c.262-44_262-43insTGTTG XP_006721011.1:n.262-44_262-43insTGTTG
NM_024589.3:c.532-44_532-43insTGTTG MANE Select NP_078865.1:n.532-44_532-43insTGTTG
NR_046480.2:n.539-44_539-43insTGTTG