Canonical Allele Identifier: CA394653362

Gene: ROGDI

Linked Data

• MyVariant Identifiers: chr16:g.4849733C>G (hg19) ; chr16:g.4799732C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4799732C>G , CM000678.2:g.4799732C>G	GRCh38
NC_000016.9:g.4849733C>G , CM000678.1:g.4849733C>G	GRCh37
NC_000016.8:g.4789734C>G	NCBI36
NG_032174.1:g.8219G>C , LRG_455:g.8219G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.386G>C MANE Select	ENSP00000322832.6:p.Ser129Thr
ENST00000322048.11:c.386G>C	ENSP00000322832.5:p.Ser129Thr
ENST00000585653.1:n.518G>C
ENST00000586153.1:c.131G>C	ENSP00000464699.1:p.Ser44Thr
ENST00000586336.5:n.485G>C
ENST00000586504.5:c.166G>C
ENST00000587377.5:c.386G>C	ENSP00000468343.1:p.Ser129Thr
ENST00000587711.5:c.118-1065G>C	ENSP00000467459.1:n.118-1065G>C
ENST00000587843.5:c.*124G>C	ENSP00000465970.1:n.*124G>C
ENST00000588201.5:c.*243G>C	ENSP00000466529.1:n.*243G>C
ENST00000589543.5:n.343G>C
ENST00000591292.5:n.1715G>C
ENST00000591392.5:c.314G>C	ENSP00000467509.1:p.Ser105Thr
ENST00000592019.1:c.76+29G>C
NM_024589.2:c.386G>C , LRG_455t1:c.386G>C	NP_078865.1:p.Ser129Thr
NR_046480.1:n.710G>C
XM_006720947.2:c.386G>C	XP_006721010.1:p.Ser129Thr
XM_006720948.2:c.116G>C	XP_006721011.1:p.Ser39Thr
XM_006720947.4:c.386G>C	XP_006721010.1:p.Ser129Thr
XM_006720948.4:c.116G>C	XP_006721011.1:p.Ser39Thr
NM_024589.3:c.386G>C MANE Select	NP_078865.1:p.Ser129Thr
NR_046480.2:n.393G>C