Canonical Allele Identifier: CA2203530262

Gene: ROGDI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4799703_4799704delinsCC , CM000678.2:g.4799703_4799704delinsCC	GRCh38
NC_000016.9:g.4849704_4849705delinsCC , CM000678.1:g.4849704_4849705delinsCC	GRCh37
NC_000016.8:g.4789705_4789706delinsCC	NCBI36
NG_032174.1:g.8247_8248delinsGG , LRG_455:g.8247_8248delinsGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.414_415delinsGG MANE Select	ENSP00000322832.6:p.Thr138=
ENST00000322048.11:c.414_415delinsGG	ENSP00000322832.5:p.Thr138=
ENST00000585653.1:n.546_547delinsGG
ENST00000586153.1:c.159_160delinsGG	ENSP00000464699.1:p.Thr53=
ENST00000586336.5:n.513_514delinsGG
ENST00000586504.5:c.194_195delinsGG
ENST00000587377.5:c.414_415delinsGG	ENSP00000468343.1:p.Thr138=
ENST00000587711.5:c.118-1037_118-1036delinsGG	ENSP00000467459.1:n.118-1037_118-1036delinsGG
ENST00000587843.5:c.*152_*153delinsGG	ENSP00000465970.1:n.*152_*153delinsGG
ENST00000588201.5:c.*271_*272delinsGG	ENSP00000466529.1:n.*271_*272delinsGG
ENST00000589543.5:n.371_372delinsGG
ENST00000591292.5:n.1743_1744delinsGG
ENST00000591392.5:c.342_343delinsGG	ENSP00000467509.1:p.Thr114=
ENST00000592019.1:c.76+57_76+58delinsGG
NM_024589.2:c.414_415delinsGG , LRG_455t1:c.414_415delinsGG	NP_078865.1:p.Thr138=
NR_046480.1:n.738_739delinsGG
XM_006720947.2:c.414_415delinsGG	XP_006721010.1:p.Thr138=
XM_006720948.2:c.144_145delinsGG	XP_006721011.1:p.Thr48=
XM_006720947.4:c.414_415delinsGG	XP_006721010.1:p.Thr138=
XM_006720948.4:c.144_145delinsGG	XP_006721011.1:p.Thr48=
NM_024589.3:c.414_415delinsGG MANE Select	NP_078865.1:p.Thr138=
NR_046480.2:n.421_422delinsGG