Canonical Allele Identifier: CA394653276

Gene: ROGDI

Linked Data

• MyVariant Identifiers: chr16:g.4849716G>C (hg19) ; chr16:g.4799715G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4799715G>C , CM000678.2:g.4799715G>C	GRCh38
NC_000016.9:g.4849716G>C , CM000678.1:g.4849716G>C	GRCh37
NC_000016.8:g.4789717G>C	NCBI36
NG_032174.1:g.8236C>G , LRG_455:g.8236C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.403C>G MANE Select	ENSP00000322832.6:p.Gln135Glu
ENST00000322048.11:c.403C>G	ENSP00000322832.5:p.Gln135Glu
ENST00000585653.1:n.535C>G
ENST00000586153.1:c.148C>G	ENSP00000464699.1:p.Gln50Glu
ENST00000586336.5:n.502C>G
ENST00000586504.5:c.183C>G
ENST00000587377.5:c.403C>G	ENSP00000468343.1:p.Gln135Glu
ENST00000587711.5:c.118-1048C>G	ENSP00000467459.1:n.118-1048C>G
ENST00000587843.5:c.*141C>G	ENSP00000465970.1:n.*141C>G
ENST00000588201.5:c.*260C>G	ENSP00000466529.1:n.*260C>G
ENST00000589543.5:n.360C>G
ENST00000591292.5:n.1732C>G
ENST00000591392.5:c.331C>G	ENSP00000467509.1:p.Gln111Glu
ENST00000592019.1:c.76+46C>G
NM_024589.2:c.403C>G , LRG_455t1:c.403C>G	NP_078865.1:p.Gln135Glu
NR_046480.1:n.727C>G
XM_006720947.2:c.403C>G	XP_006721010.1:p.Gln135Glu
XM_006720948.2:c.133C>G	XP_006721011.1:p.Gln45Glu
XM_006720947.4:c.403C>G	XP_006721010.1:p.Gln135Glu
XM_006720948.4:c.133C>G	XP_006721011.1:p.Gln45Glu
NM_024589.3:c.403C>G MANE Select	NP_078865.1:p.Gln135Glu
NR_046480.2:n.410C>G