Canonical Allele Identifier: CA2631553056

Gene: ROGDI

Linked Data

• gnomAD v4: 16-4799640-AAGAACGTGGGACT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4799643_4799655del , CM000678.2:g.4799643_4799655del	GRCh38
NC_000016.9:g.4849644_4849656del , CM000678.1:g.4849644_4849656del	GRCh37
NC_000016.8:g.4789645_4789657del	NCBI36
NG_032174.1:g.8298_8310del , LRG_455:g.8298_8310del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.432+33_432+45del MANE Select	ENSP00000322832.6:n.432+33_432+45del
ENST00000322048.11:c.432+33_432+45del	ENSP00000322832.5:n.432+33_432+45del
ENST00000585653.1:n.564+33_564+45del
ENST00000586153.1:c.177+33_177+45del	ENSP00000464699.1:n.177+33_177+45del
ENST00000586336.5:n.531+33_531+45del
ENST00000586504.5:c.212+33_212+45del
ENST00000587377.5:c.423+42_423+54del	ENSP00000468343.1:n.423+42_423+54del
ENST00000587711.5:c.118-986_118-974del	ENSP00000467459.1:n.118-986_118-974del
ENST00000587843.5:c.*170+33_*170+45del	ENSP00000465970.1:n.*170+33_*170+45del
ENST00000588201.5:c.*289+33_*289+45del	ENSP00000466529.1:n.*289+33_*289+45del
ENST00000589543.5:n.389+33_389+45del
ENST00000591292.5:n.1761+33_1761+45del
ENST00000591392.5:c.360+33_360+45del	ENSP00000467509.1:n.360+33_360+45del
ENST00000592019.1:c.76+108_76+120del
NM_024589.2:c.432+33_432+45del , LRG_455t1:c.432+33_432+45del	NP_078865.1:n.432+33_432+45del
NR_046480.1:n.756+33_756+45del
XM_006720947.2:c.432+33_432+45del	XP_006721010.1:n.432+33_432+45del
XM_006720948.2:c.162+33_162+45del	XP_006721011.1:n.162+33_162+45del
XM_006720947.4:c.432+33_432+45del	XP_006721010.1:n.432+33_432+45del
XM_006720948.4:c.162+33_162+45del	XP_006721011.1:n.162+33_162+45del
NM_024589.3:c.432+33_432+45del MANE Select	NP_078865.1:n.432+33_432+45del
NR_046480.2:n.439+33_439+45del