Canonical Allele Identifier: CA2203530305

Gene: ROGDI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4799781T= , CM000678.2:g.4799781T=	GRCh38
NC_000016.9:g.4849782T= , CM000678.1:g.4849782T=	GRCh37
NC_000016.8:g.4789783T=	NCBI36
NG_032174.1:g.8170A= , LRG_455:g.8170A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.337A= MANE Select	ENSP00000322832.6:p.Ile113=
ENST00000322048.11:c.337A=	ENSP00000322832.5:p.Ile113=
ENST00000585653.1:n.469A=
ENST00000586153.1:c.82A=	ENSP00000464699.1:p.Ile28=
ENST00000586336.5:n.436A=
ENST00000586504.5:c.117A=
ENST00000587377.5:c.337A=	ENSP00000468343.1:p.Ile113=
ENST00000587711.5:c.118-1114A=	ENSP00000467459.1:n.118-1114A=
ENST00000587843.5:c.*75A=	ENSP00000465970.1:n.*75A=
ENST00000588201.5:c.*194A=	ENSP00000466529.1:n.*194A=
ENST00000589543.5:n.294A=
ENST00000591292.5:n.1666A=
ENST00000591392.5:c.265A=	ENSP00000467509.1:p.Ile89=
ENST00000592019.1:c.56A=
NM_024589.2:c.337A= , LRG_455t1:c.337A=	NP_078865.1:p.Ile113=
NR_046480.1:n.661A=
XM_006720947.2:c.337A=	XP_006721010.1:p.Ile113=
XM_006720948.2:c.67A=	XP_006721011.1:p.Ile23=
XM_006720947.4:c.337A=	XP_006721010.1:p.Ile113=
XM_006720948.4:c.67A=	XP_006721011.1:p.Ile23=
NM_024589.3:c.337A= MANE Select	NP_078865.1:p.Ile113=
NR_046480.2:n.344A=