Canonical Allele Identifier: CA2203528958

Gene: ROGDI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4797853_4797866delinsAGAGGGTCCCTGAG , CM000678.2:g.4797853_4797866delinsAGAGGGTCCCTGAG	GRCh38
NC_000016.9:g.4847854_4847867delinsAGAGGGTCCCTGAG , CM000678.1:g.4847854_4847867delinsAGAGGGTCCCTGAG	GRCh37
NC_000016.8:g.4787855_4787868delinsAGAGGGTCCCTGAG	NCBI36
NG_032174.1:g.10085_10098delinsCTCAGGGACCCTCT , LRG_455:g.10085_10098delinsCTCAGGGACCCTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.696-26_696-13delinsCTCAGGGACCCTCT MANE Select	ENSP00000322832.6:n.696-26_696-13delinsCTCAGGGACCCTCT
ENST00000322048.11:c.696-26_696-13delinsCTCAGGGACCCTCT	ENSP00000322832.5:n.696-26_696-13delinsCTCAGGGACCCTCT
ENST00000586153.1:c.342-30_342-17delinsCTCAGGGACCCTCT	ENSP00000464699.1:n.342-30_342-17delinsCTCAGGGACCCTCT
ENST00000586336.5:n.795-26_795-13delinsCTCAGGGACCCTCT
ENST00000586504.5:c.426-26_426-13delinsCTCAGGGACCCTCT
ENST00000587377.5:c.*16-26_*16-13delinsCTCAGGGACCCTCT	ENSP00000468343.1:n.*16-26_*16-13delinsCTCAGGGACCCTCT
ENST00000587711.5:c.381-26_381-13delinsCTCAGGGACCCTCT	ENSP00000467459.1:n.381-26_381-13delinsCTCAGGGACCCTCT
ENST00000587843.5:c.*434-26_*434-13delinsCTCAGGGACCCTCT	ENSP00000465970.1:n.*434-26_*434-13delinsCTCAGGGACCCTCT
ENST00000588201.5:c.*687-26_*687-13delinsCTCAGGGACCCTCT	ENSP00000466529.1:n.*687-26_*687-13delinsCTCAGGGACCCTCT
ENST00000589543.5:n.653-26_653-13delinsCTCAGGGACCCTCT
ENST00000591292.5:n.2025-26_2025-13delinsCTCAGGGACCCTCT
ENST00000591392.5:c.624-26_624-13delinsCTCAGGGACCCTCT	ENSP00000467509.1:n.624-26_624-13delinsCTCAGGGACCCTCT
ENST00000592019.1:c.77-51_77-38delinsCTCAGGGACCCTCT
NM_024589.2:c.696-26_696-13delinsCTCAGGGACCCTCT , LRG_455t1:c.696-26_696-13delinsCTCAGGGACCCTCT	NP_078865.1:n.696-26_696-13delinsCTCAGGGACCCTCT
NR_046480.1:n.1020-26_1020-13delinsCTCAGGGACCCTCT
XM_006720947.2:c.696-5_704delinsCTCAGGGACCCTCT
XM_006720948.2:c.426-5_434delinsCTCAGGGACCCTCT
XM_006720947.4:c.696-5_704delinsCTCAGGGACCCTCT
XM_006720948.4:c.426-5_434delinsCTCAGGGACCCTCT
NM_024589.3:c.696-26_696-13delinsCTCAGGGACCCTCT MANE Select	NP_078865.1:n.696-26_696-13delinsCTCAGGGACCCTCT
NR_046480.2:n.703-26_703-13delinsCTCAGGGACCCTCT