Canonical Allele Identifier: CA394653412

Gene: ROGDI

Linked Data

• MyVariant Identifiers: chr16:g.4849739A>G (hg19) ; chr16:g.4799738A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4799738A>G , CM000678.2:g.4799738A>G	GRCh38
NC_000016.9:g.4849739A>G , CM000678.1:g.4849739A>G	GRCh37
NC_000016.8:g.4789740A>G	NCBI36
NG_032174.1:g.8213T>C , LRG_455:g.8213T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.380T>C MANE Select	ENSP00000322832.6:p.Leu127Pro
ENST00000322048.11:c.380T>C	ENSP00000322832.5:p.Leu127Pro
ENST00000585653.1:n.512T>C
ENST00000586153.1:c.125T>C	ENSP00000464699.1:p.Leu42Pro
ENST00000586336.5:n.479T>C
ENST00000586504.5:c.160T>C
ENST00000587377.5:c.380T>C	ENSP00000468343.1:p.Leu127Pro
ENST00000587711.5:c.118-1071T>C	ENSP00000467459.1:n.118-1071T>C
ENST00000587843.5:c.*118T>C	ENSP00000465970.1:n.*118T>C
ENST00000588201.5:c.*237T>C	ENSP00000466529.1:n.*237T>C
ENST00000589543.5:n.337T>C
ENST00000591292.5:n.1709T>C
ENST00000591392.5:c.308T>C	ENSP00000467509.1:p.Leu103Pro
ENST00000592019.1:c.76+23T>C
NM_024589.2:c.380T>C , LRG_455t1:c.380T>C	NP_078865.1:p.Leu127Pro
NR_046480.1:n.704T>C
XM_006720947.2:c.380T>C	XP_006721010.1:p.Leu127Pro
XM_006720948.2:c.110T>C	XP_006721011.1:p.Leu37Pro
XM_006720947.4:c.380T>C	XP_006721010.1:p.Leu127Pro
XM_006720948.4:c.110T>C	XP_006721011.1:p.Leu37Pro
NM_024589.3:c.380T>C MANE Select	NP_078865.1:p.Leu127Pro
NR_046480.2:n.387T>C