Canonical Allele Identifier: CA2203530284

Gene: ROGDI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4799732C= , CM000678.2:g.4799732C=	GRCh38
NC_000016.9:g.4849733C= , CM000678.1:g.4849733C=	GRCh37
NC_000016.8:g.4789734C=	NCBI36
NG_032174.1:g.8219G= , LRG_455:g.8219G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.386G= MANE Select	ENSP00000322832.6:p.Ser129=
ENST00000322048.11:c.386G=	ENSP00000322832.5:p.Ser129=
ENST00000585653.1:n.518G=
ENST00000586153.1:c.131G=	ENSP00000464699.1:p.Ser44=
ENST00000586336.5:n.485G=
ENST00000586504.5:c.166G=
ENST00000587377.5:c.386G=	ENSP00000468343.1:p.Ser129=
ENST00000587711.5:c.118-1065G=	ENSP00000467459.1:n.118-1065G=
ENST00000587843.5:c.*124G=	ENSP00000465970.1:n.*124G=
ENST00000588201.5:c.*243G=	ENSP00000466529.1:n.*243G=
ENST00000589543.5:n.343G=
ENST00000591292.5:n.1715G=
ENST00000591392.5:c.314G=	ENSP00000467509.1:p.Ser105=
ENST00000592019.1:c.76+29G=
NM_024589.2:c.386G= , LRG_455t1:c.386G=	NP_078865.1:p.Ser129=
NR_046480.1:n.710G=
XM_006720947.2:c.386G=	XP_006721010.1:p.Ser129=
XM_006720948.2:c.116G=	XP_006721011.1:p.Ser39=
XM_006720947.4:c.386G=	XP_006721010.1:p.Ser129=
XM_006720948.4:c.116G=	XP_006721011.1:p.Ser39=
NM_024589.3:c.386G= MANE Select	NP_078865.1:p.Ser129=
NR_046480.2:n.393G=