Canonical Allele Identifier: CA394649409

Gene: ROGDI

Linked Data

• MyVariant Identifiers: chr16:g.4847951G>C (hg19) ; chr16:g.4797950G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4797950G>C , CM000678.2:g.4797950G>C	GRCh38
NC_000016.9:g.4847951G>C , CM000678.1:g.4847951G>C	GRCh37
NC_000016.8:g.4787952G>C	NCBI36
NG_032174.1:g.10001C>G , LRG_455:g.10001C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.683C>G MANE Select	ENSP00000322832.6:p.Pro228Arg
ENST00000322048.11:c.683C>G	ENSP00000322832.5:p.Pro228Arg
ENST00000586153.1:c.329C>G	ENSP00000464699.1:p.Pro110Arg
ENST00000586336.5:n.782C>G
ENST00000586504.5:c.426-110C>G
ENST00000587377.5:c.*3C>G	ENSP00000468343.1:n.*3C>G
ENST00000587711.5:c.368C>G	ENSP00000467459.1:p.Pro123Arg
ENST00000587843.5:c.*421C>G	ENSP00000465970.1:n.*421C>G
ENST00000588201.5:c.*674C>G	ENSP00000466529.1:n.*674C>G
ENST00000589543.5:n.640C>G
ENST00000591292.5:n.2012C>G
ENST00000591392.5:c.611C>G	ENSP00000467509.1:p.Pro204Arg
ENST00000592019.1:c.77-135C>G
NM_024589.2:c.683C>G , LRG_455t1:c.683C>G	NP_078865.1:p.Pro228Arg
NR_046480.1:n.1007C>G
XM_006720947.2:c.683C>G	XP_006721010.1:p.Pro228Arg
XM_006720948.2:c.413C>G	XP_006721011.1:p.Pro138Arg
XM_006720947.4:c.683C>G	XP_006721010.1:p.Pro228Arg
XM_006720948.4:c.413C>G	XP_006721011.1:p.Pro138Arg
NM_024589.3:c.683C>G MANE Select	NP_078865.1:p.Pro228Arg
NR_046480.2:n.690C>G