Canonical Allele Identifier: CA394653569

Gene: ROGDI

Linked Data

• MyVariant Identifiers: chr16:g.4849764G>C (hg19) ; chr16:g.4799763G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4799763G>C , CM000678.2:g.4799763G>C	GRCh38
NC_000016.9:g.4849764G>C , CM000678.1:g.4849764G>C	GRCh37
NC_000016.8:g.4789765G>C	NCBI36
NG_032174.1:g.8188C>G , LRG_455:g.8188C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.355C>G MANE Select	ENSP00000322832.6:p.His119Asp
ENST00000322048.11:c.355C>G	ENSP00000322832.5:p.His119Asp
ENST00000585653.1:n.487C>G
ENST00000586153.1:c.100C>G	ENSP00000464699.1:p.His34Asp
ENST00000586336.5:n.454C>G
ENST00000586504.5:c.135C>G
ENST00000587377.5:c.355C>G	ENSP00000468343.1:p.His119Asp
ENST00000587711.5:c.118-1096C>G	ENSP00000467459.1:n.118-1096C>G
ENST00000587843.5:c.*93C>G	ENSP00000465970.1:n.*93C>G
ENST00000588201.5:c.*212C>G	ENSP00000466529.1:n.*212C>G
ENST00000589543.5:n.312C>G
ENST00000591292.5:n.1684C>G
ENST00000591392.5:c.283C>G	ENSP00000467509.1:p.His95Asp
ENST00000592019.1:c.74C>G
NM_024589.2:c.355C>G , LRG_455t1:c.355C>G	NP_078865.1:p.His119Asp
NR_046480.1:n.679C>G
XM_006720947.2:c.355C>G	XP_006721010.1:p.His119Asp
XM_006720948.2:c.85C>G	XP_006721011.1:p.His29Asp
XM_006720947.4:c.355C>G	XP_006721010.1:p.His119Asp
XM_006720948.4:c.85C>G	XP_006721011.1:p.His29Asp
NM_024589.3:c.355C>G MANE Select	NP_078865.1:p.His119Asp
NR_046480.2:n.362C>G