Canonical Allele Identifier: CA394656550
Community Standard Title: NM_024589.3(ROGDI):c.103C>T (p.Gln35Ter)
Gene: ROGDI HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.4802396G>A , CM000678.2:g.4802396G>A GRCh38
NC_000016.9:g.4852397G>A , CM000678.1:g.4852397G>A GRCh37
NC_000016.8:g.4792398G>A NCBI36
NG_032174.1:g.5555C>T , LRG_455:g.5555C>T

Transcript Alleles

HGVS Amino-acid Change
NM_024589.3:c.103C>T MANE Select NP_078865.1:p.Gln35Ter
ENST00000322048.12:c.103C>T MANE Select ENSP00000322832.6:p.Gln35Ter
NM_024589.2:c.103C>T , LRG_455t1:c.103C>T NP_078865.1:p.Gln35Ter
NR_046480.1:n.482C>T
NR_046480.2:n.165C>T
ENST00000322048.11:c.103C>T ENSP00000322832.5:p.Gln35Ter
ENST00000585653.1:n.235C>T
ENST00000585871.1:n.412C>T
ENST00000587377.5:c.103C>T ENSP00000468343.1:p.Gln35Ter
ENST00000587711.5:c.103C>T ENSP00000467459.1:p.Gln35Ter
ENST00000587843.5:c.103C>T ENSP00000465970.1:p.Gln35Ter
ENST00000588201.5:c.103C>T ENSP00000466529.1:p.Gln35Ter
ENST00000590198.1:n.270C>T
ENST00000591392.5:c.45+131C>T ENSP00000467509.1:n.45+131C>T
ENST00000592112.1:n.388C>T
XM_006720947.2:c.103C>T XP_006721010.1:p.Gln35Ter
XM_006720947.4:c.103C>T XP_006721010.1:p.Gln35Ter
XM_006720948.2:c.-113C>T XP_006721011.1:n.-113C>T
XM_006720948.4:c.-113C>T XP_006721011.1:n.-113C>T