Canonical Allele Identifier: CA2203529012

Gene: ROGDI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4797915_4797916delinsAC , CM000678.2:g.4797915_4797916delinsAC	GRCh38
NC_000016.9:g.4847916_4847917delinsAC , CM000678.1:g.4847916_4847917delinsAC	GRCh37
NC_000016.8:g.4787917_4787918delinsAC	NCBI36
NG_032174.1:g.10035_10036delinsGT , LRG_455:g.10035_10036delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.695+22_695+23delinsGT MANE Select	ENSP00000322832.6:n.695+22_695+23delinsGT
ENST00000322048.11:c.695+22_695+23delinsGT	ENSP00000322832.5:n.695+22_695+23delinsGT
ENST00000586153.1:c.341+22_341+23delinsGT	ENSP00000464699.1:n.341+22_341+23delinsGT
ENST00000586336.5:n.794+22_794+23delinsGT
ENST00000586504.5:c.426-76_426-75delinsGT
ENST00000587377.5:c.*15+22_*15+23delinsGT	ENSP00000468343.1:n.*15+22_*15+23delinsGT
ENST00000587711.5:c.380+22_380+23delinsGT	ENSP00000467459.1:n.380+22_380+23delinsGT
ENST00000587843.5:c.*433+22_*433+23delinsGT	ENSP00000465970.1:n.*433+22_*433+23delinsGT
ENST00000588201.5:c.*686+22_*686+23delinsGT	ENSP00000466529.1:n.*686+22_*686+23delinsGT
ENST00000589543.5:n.652+22_652+23delinsGT
ENST00000591292.5:n.2024+22_2024+23delinsGT
ENST00000591392.5:c.623+22_623+23delinsGT	ENSP00000467509.1:n.623+22_623+23delinsGT
ENST00000592019.1:c.77-101_77-100delinsGT
NM_024589.2:c.695+22_695+23delinsGT , LRG_455t1:c.695+22_695+23delinsGT	NP_078865.1:n.695+22_695+23delinsGT
NR_046480.1:n.1019+22_1019+23delinsGT
XM_006720947.2:c.695+22_695+23delinsGT	XP_006721010.1:n.695+22_695+23delinsGT
XM_006720948.2:c.425+22_425+23delinsGT	XP_006721011.1:n.425+22_425+23delinsGT
XM_006720947.4:c.695+22_695+23delinsGT	XP_006721010.1:n.695+22_695+23delinsGT
XM_006720948.4:c.425+22_425+23delinsGT	XP_006721011.1:n.425+22_425+23delinsGT
NM_024589.3:c.695+22_695+23delinsGT MANE Select	NP_078865.1:n.695+22_695+23delinsGT
NR_046480.2:n.702+22_702+23delinsGT