Canonical Allele Identifier: CA394653602

Gene: ROGDI

Linked Data

• MyVariant Identifiers: chr16:g.4849767T>A (hg19) ; chr16:g.4799766T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4799766T>A , CM000678.2:g.4799766T>A	GRCh38
NC_000016.9:g.4849767T>A , CM000678.1:g.4849767T>A	GRCh37
NC_000016.8:g.4789768T>A	NCBI36
NG_032174.1:g.8185A>T , LRG_455:g.8185A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.352A>T MANE Select	ENSP00000322832.6:p.Asn118Tyr
ENST00000322048.11:c.352A>T	ENSP00000322832.5:p.Asn118Tyr
ENST00000585653.1:n.484A>T
ENST00000586153.1:c.97A>T	ENSP00000464699.1:p.Asn33Tyr
ENST00000586336.5:n.451A>T
ENST00000586504.5:c.132A>T
ENST00000587377.5:c.352A>T	ENSP00000468343.1:p.Asn118Tyr
ENST00000587711.5:c.118-1099A>T	ENSP00000467459.1:n.118-1099A>T
ENST00000587843.5:c.*90A>T	ENSP00000465970.1:n.*90A>T
ENST00000588201.5:c.*209A>T	ENSP00000466529.1:n.*209A>T
ENST00000589543.5:n.309A>T
ENST00000591292.5:n.1681A>T
ENST00000591392.5:c.280A>T	ENSP00000467509.1:p.Asn94Tyr
ENST00000592019.1:c.71A>T
NM_024589.2:c.352A>T , LRG_455t1:c.352A>T	NP_078865.1:p.Asn118Tyr
NR_046480.1:n.676A>T
XM_006720947.2:c.352A>T	XP_006721010.1:p.Asn118Tyr
XM_006720948.2:c.82A>T	XP_006721011.1:p.Asn28Tyr
XM_006720947.4:c.352A>T	XP_006721010.1:p.Asn118Tyr
XM_006720948.4:c.82A>T	XP_006721011.1:p.Asn28Tyr
NM_024589.3:c.352A>T MANE Select	NP_078865.1:p.Asn118Tyr
NR_046480.2:n.359A>T