Canonical Allele Identifier: CA2203530288

Gene: ROGDI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4799743G= , CM000678.2:g.4799743G=	GRCh38
NC_000016.9:g.4849744G= , CM000678.1:g.4849744G=	GRCh37
NC_000016.8:g.4789745G=	NCBI36
NG_032174.1:g.8208C= , LRG_455:g.8208C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.375C= MANE Select	ENSP00000322832.6:p.Tyr125=
ENST00000322048.11:c.375C=	ENSP00000322832.5:p.Tyr125=
ENST00000585653.1:n.507C=
ENST00000586153.1:c.120C=	ENSP00000464699.1:p.Tyr40=
ENST00000586336.5:n.474C=
ENST00000586504.5:c.155C=
ENST00000587377.5:c.375C=	ENSP00000468343.1:p.Tyr125=
ENST00000587711.5:c.118-1076C=	ENSP00000467459.1:n.118-1076C=
ENST00000587843.5:c.*113C=	ENSP00000465970.1:n.*113C=
ENST00000588201.5:c.*232C=	ENSP00000466529.1:n.*232C=
ENST00000589543.5:n.332C=
ENST00000591292.5:n.1704C=
ENST00000591392.5:c.303C=	ENSP00000467509.1:p.Tyr101=
ENST00000592019.1:c.76+18C=
NM_024589.2:c.375C= , LRG_455t1:c.375C=	NP_078865.1:p.Tyr125=
NR_046480.1:n.699C=
XM_006720947.2:c.375C=	XP_006721010.1:p.Tyr125=
XM_006720948.2:c.105C=	XP_006721011.1:p.Tyr35=
XM_006720947.4:c.375C=	XP_006721010.1:p.Tyr125=
XM_006720948.4:c.105C=	XP_006721011.1:p.Tyr35=
NM_024589.3:c.375C= MANE Select	NP_078865.1:p.Tyr125=
NR_046480.2:n.382C=