Canonical Allele Identifier: CA2203530338

Gene: ROGDI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4799820C= , CM000678.2:g.4799820C=	GRCh38
NC_000016.9:g.4849821C= , CM000678.1:g.4849821C=	GRCh37
NC_000016.8:g.4789822C=	NCBI36
NG_032174.1:g.8131G= , LRG_455:g.8131G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.337-39G= MANE Select	ENSP00000322832.6:n.337-39G=
ENST00000322048.11:c.337-39G=	ENSP00000322832.5:n.337-39G=
ENST00000585653.1:n.469-39G=
ENST00000586153.1:c.82-39G=	ENSP00000464699.1:n.82-39G=
ENST00000586336.5:n.436-39G=
ENST00000586504.5:c.117-39G=
ENST00000587377.5:c.337-39G=	ENSP00000468343.1:n.337-39G=
ENST00000587711.5:c.118-1153G=	ENSP00000467459.1:n.118-1153G=
ENST00000587843.5:c.*75-39G=	ENSP00000465970.1:n.*75-39G=
ENST00000588201.5:c.*194-39G=	ENSP00000466529.1:n.*194-39G=
ENST00000589543.5:n.294-39G=
ENST00000591292.5:n.1666-39G=
ENST00000591392.5:c.265-39G=	ENSP00000467509.1:n.265-39G=
ENST00000592019.1:c.56-39G=
NM_024589.2:c.337-39G= , LRG_455t1:c.337-39G=	NP_078865.1:n.337-39G=
NR_046480.1:n.661-39G=
XM_006720947.2:c.337-39G=	XP_006721010.1:n.337-39G=
XM_006720948.2:c.67-39G=	XP_006721011.1:n.67-39G=
XM_006720947.4:c.337-39G=	XP_006721010.1:n.337-39G=
XM_006720948.4:c.67-39G=	XP_006721011.1:n.67-39G=
NM_024589.3:c.337-39G= MANE Select	NP_078865.1:n.337-39G=
NR_046480.2:n.344-39G=