Canonical Allele Identifier: CA2203530235

Gene: ROGDI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4799665_4799677delinsTCAGGCCCGGGGG , CM000678.2:g.4799665_4799677delinsTCAGGCCCGGGGG	GRCh38
NC_000016.9:g.4849666_4849678delinsTCAGGCCCGGGGG , CM000678.1:g.4849666_4849678delinsTCAGGCCCGGGGG	GRCh37
NC_000016.8:g.4789667_4789679delinsTCAGGCCCGGGGG	NCBI36
NG_032174.1:g.8274_8286delinsCCCCCGGGCCTGA , LRG_455:g.8274_8286delinsCCCCCGGGCCTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.432+9_432+21delinsCCCCCGGGCCTGA MANE Select	ENSP00000322832.6:n.432+9_432+21delinsCCCCCGGGCCTGA
ENST00000322048.11:c.432+9_432+21delinsCCCCCGGGCCTGA	ENSP00000322832.5:n.432+9_432+21delinsCCCCCGGGCCTGA
ENST00000585653.1:n.564+9_564+21delinsCCCCCGGGCCTGA
ENST00000586153.1:c.177+9_177+21delinsCCCCCGGGCCTGA	ENSP00000464699.1:n.177+9_177+21delinsCCCCCGGGCCTGA
ENST00000586336.5:n.531+9_531+21delinsCCCCCGGGCCTGA
ENST00000586504.5:c.212+9_212+21delinsCCCCCGGGCCTGA
ENST00000587377.5:c.423+18_423+30delinsCCCCCGGGCCTGA	ENSP00000468343.1:n.423+18_423+30delinsCCCCCGGGCCTGA
ENST00000587711.5:c.118-1010_118-998delinsCCCCCGGGCCTGA	ENSP00000467459.1:n.118-1010_118-998delinsCCCCCGGGCCTGA
ENST00000587843.5:c.*170+9_*170+21delinsCCCCCGGGCCTGA	ENSP00000465970.1:n.*170+9_*170+21delinsCCCCCGGGCCTGA
ENST00000588201.5:c.*289+9_*289+21delinsCCCCCGGGCCTGA	ENSP00000466529.1:n.*289+9_*289+21delinsCCCCCGGGCCTGA
ENST00000589543.5:n.389+9_389+21delinsCCCCCGGGCCTGA
ENST00000591292.5:n.1761+9_1761+21delinsCCCCCGGGCCTGA
ENST00000591392.5:c.360+9_360+21delinsCCCCCGGGCCTGA	ENSP00000467509.1:n.360+9_360+21delinsCCCCCGGGCCTGA
ENST00000592019.1:c.76+84_76+96delinsCCCCCGGGCCTGA
NM_024589.2:c.432+9_432+21delinsCCCCCGGGCCTGA , LRG_455t1:c.432+9_432+21delinsCCCCCGGGCCTGA	NP_078865.1:n.432+9_432+21delinsCCCCCGGGCCTGA
NR_046480.1:n.756+9_756+21delinsCCCCCGGGCCTGA
XM_006720947.2:c.432+9_432+21delinsCCCCCGGGCCTGA	XP_006721010.1:n.432+9_432+21delinsCCCCCGGGCCTGA
XM_006720948.2:c.162+9_162+21delinsCCCCCGGGCCTGA	XP_006721011.1:n.162+9_162+21delinsCCCCCGGGCCTGA
XM_006720947.4:c.432+9_432+21delinsCCCCCGGGCCTGA	XP_006721010.1:n.432+9_432+21delinsCCCCCGGGCCTGA
XM_006720948.4:c.162+9_162+21delinsCCCCCGGGCCTGA	XP_006721011.1:n.162+9_162+21delinsCCCCCGGGCCTGA
NM_024589.3:c.432+9_432+21delinsCCCCCGGGCCTGA MANE Select	NP_078865.1:n.432+9_432+21delinsCCCCCGGGCCTGA
NR_046480.2:n.439+9_439+21delinsCCCCCGGGCCTGA