Canonical Allele Identifier: CA2203529121
Gene: ROGDI HGNC NCBI

Linked Data

dbSNP Id: rs2082675162

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.4798051_4798054dup , CM000678.2:g.4798051_4798054dup GRCh38
NC_000016.9:g.4848052_4848055dup , CM000678.1:g.4848052_4848055dup GRCh37
NC_000016.8:g.4788053_4788056dup NCBI36
NG_032174.1:g.9898_9901dup , LRG_455:g.9898_9901dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000322048.12:c.645+18_645+21dup MANE Select ENSP00000322832.6:n.645+18_645+21dup
ENST00000322048.11:c.645+18_645+21dup ENSP00000322832.5:n.645+18_645+21dup
ENST00000586153.1:c.291+18_291+21dup ENSP00000464699.1:n.291+18_291+21dup
ENST00000586336.5:n.744+18_744+21dup
ENST00000586504.5:c.425+18_425+21dup
ENST00000587377.5:c.658+18_658+21dup ENSP00000468343.1:n.658+18_658+21dup
ENST00000587711.5:c.330+18_330+21dup ENSP00000467459.1:n.330+18_330+21dup
ENST00000587843.5:c.*383+18_*383+21dup ENSP00000465970.1:n.*383+18_*383+21dup
ENST00000588201.5:c.*636+18_*636+21dup ENSP00000466529.1:n.*636+18_*636+21dup
ENST00000589543.5:n.602+18_602+21dup
ENST00000591292.5:n.1974+18_1974+21dup
ENST00000591392.5:c.573+18_573+21dup ENSP00000467509.1:n.573+18_573+21dup
ENST00000592019.1:c.77-238_77-235dup
NM_024589.2:c.645+18_645+21dup , LRG_455t1:c.645+18_645+21dup NP_078865.1:n.645+18_645+21dup
NR_046480.1:n.969+18_969+21dup
XM_006720947.2:c.645+18_645+21dup XP_006721010.1:n.645+18_645+21dup
XM_006720948.2:c.375+18_375+21dup XP_006721011.1:n.375+18_375+21dup
XM_006720947.4:c.645+18_645+21dup XP_006721010.1:n.645+18_645+21dup
XM_006720948.4:c.375+18_375+21dup XP_006721011.1:n.375+18_375+21dup
NM_024589.3:c.645+18_645+21dup MANE Select NP_078865.1:n.645+18_645+21dup
NR_046480.2:n.652+18_652+21dup