Canonical Allele Identifier: CA394653714

Gene: ROGDI

Linked Data

• dbSNP Id: rs2082695159
• MyVariant Identifiers: chr16:g.4849783C>T (hg19) ; chr16:g.4799782C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4799782C>T , CM000678.2:g.4799782C>T	GRCh38
NC_000016.9:g.4849783C>T , CM000678.1:g.4849783C>T	GRCh37
NC_000016.8:g.4789784C>T	NCBI36
NG_032174.1:g.8169G>A , LRG_455:g.8169G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.337-1G>A MANE Select	ENSP00000322832.6:n.337-1G>A
ENST00000322048.11:c.337-1G>A	ENSP00000322832.5:n.337-1G>A
ENST00000585653.1:n.469-1G>A
ENST00000586153.1:c.82-1G>A	ENSP00000464699.1:n.82-1G>A
ENST00000586336.5:n.436-1G>A
ENST00000586504.5:c.117-1G>A
ENST00000587377.5:c.337-1G>A	ENSP00000468343.1:n.337-1G>A
ENST00000587711.5:c.118-1115G>A	ENSP00000467459.1:n.118-1115G>A
ENST00000587843.5:c.*75-1G>A	ENSP00000465970.1:n.*75-1G>A
ENST00000588201.5:c.*194-1G>A	ENSP00000466529.1:n.*194-1G>A
ENST00000589543.5:n.294-1G>A
ENST00000591292.5:n.1666-1G>A
ENST00000591392.5:c.265-1G>A	ENSP00000467509.1:n.265-1G>A
ENST00000592019.1:c.56-1G>A
NM_024589.2:c.337-1G>A , LRG_455t1:c.337-1G>A	NP_078865.1:n.337-1G>A
NR_046480.1:n.661-1G>A
XM_006720947.2:c.337-1G>A	XP_006721010.1:n.337-1G>A
XM_006720948.2:c.67-1G>A	XP_006721011.1:n.67-1G>A
XM_006720947.4:c.337-1G>A	XP_006721010.1:n.337-1G>A
XM_006720948.4:c.67-1G>A	XP_006721011.1:n.67-1G>A
NM_024589.3:c.337-1G>A MANE Select	NP_078865.1:n.337-1G>A
NR_046480.2:n.344-1G>A