Canonical Allele Identifier: CA2203530271

Gene: ROGDI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4799714T= , CM000678.2:g.4799714T=	GRCh38
NC_000016.9:g.4849715T= , CM000678.1:g.4849715T=	GRCh37
NC_000016.8:g.4789716T=	NCBI36
NG_032174.1:g.8237A= , LRG_455:g.8237A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.404A= MANE Select	ENSP00000322832.6:p.Gln135=
ENST00000322048.11:c.404A=	ENSP00000322832.5:p.Gln135=
ENST00000585653.1:n.536A=
ENST00000586153.1:c.149A=	ENSP00000464699.1:p.Gln50=
ENST00000586336.5:n.503A=
ENST00000586504.5:c.184A=
ENST00000587377.5:c.404A=	ENSP00000468343.1:p.Gln135=
ENST00000587711.5:c.118-1047A=	ENSP00000467459.1:n.118-1047A=
ENST00000587843.5:c.*142A=	ENSP00000465970.1:n.*142A=
ENST00000588201.5:c.*261A=	ENSP00000466529.1:n.*261A=
ENST00000589543.5:n.361A=
ENST00000591292.5:n.1733A=
ENST00000591392.5:c.332A=	ENSP00000467509.1:p.Gln111=
ENST00000592019.1:c.76+47A=
NM_024589.2:c.404A= , LRG_455t1:c.404A=	NP_078865.1:p.Gln135=
NR_046480.1:n.728A=
XM_006720947.2:c.404A=	XP_006721010.1:p.Gln135=
XM_006720948.2:c.134A=	XP_006721011.1:p.Gln45=
XM_006720947.4:c.404A=	XP_006721010.1:p.Gln135=
XM_006720948.4:c.134A=	XP_006721011.1:p.Gln45=
NM_024589.3:c.404A= MANE Select	NP_078865.1:p.Gln135=
NR_046480.2:n.411A=