Canonical Allele Identifier: CA277137899

Gene: ROGDI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4799716G>T , CM000678.2:g.4799716G>T	GRCh38
NC_000016.9:g.4849717G>T , CM000678.1:g.4849717G>T	GRCh37
NC_000016.8:g.4789718G>T	NCBI36
NG_032174.1:g.8235C>A , LRG_455:g.8235C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_024589.3:c.402C>A MANE Select	NP_078865.1:p.Tyr134Ter
ENST00000322048.12:c.402C>A MANE Select	ENSP00000322832.6:p.Tyr134Ter
NM_024589.2:c.402C>A , LRG_455t1:c.402C>A	NP_078865.1:p.Tyr134Ter
NR_046480.1:n.726C>A
NR_046480.2:n.409C>A
ENST00000322048.11:c.402C>A	ENSP00000322832.5:p.Tyr134Ter
ENST00000585653.1:n.534C>A
ENST00000586153.1:c.147C>A	ENSP00000464699.1:p.Tyr49Ter
ENST00000586336.5:n.501C>A
ENST00000586504.5:c.182C>A
ENST00000587377.5:c.402C>A	ENSP00000468343.1:p.Tyr134Ter
ENST00000587711.5:c.118-1049C>A	ENSP00000467459.1:n.118-1049C>A
ENST00000587843.5:c.*140C>A	ENSP00000465970.1:n.*140C>A
ENST00000588201.5:c.*259C>A	ENSP00000466529.1:n.*259C>A
ENST00000589543.5:n.359C>A
ENST00000591292.5:n.1731C>A
ENST00000591392.5:c.330C>A	ENSP00000467509.1:p.Tyr110Ter
ENST00000592019.1:c.76+45C>A
XM_006720947.2:c.402C>A	XP_006721010.1:p.Tyr134Ter
XM_006720947.4:c.402C>A	XP_006721010.1:p.Tyr134Ter
XM_006720948.2:c.132C>A	XP_006721011.1:p.Tyr44Ter
XM_006720948.4:c.132C>A	XP_006721011.1:p.Tyr44Ter