Canonical Allele Identifier: CA2805667702

Gene: ROGDI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4798373A>G , CM000678.2:g.4798373A>G	GRCh38
NC_000016.9:g.4848374A>G , CM000678.1:g.4848374A>G	GRCh37
NC_000016.8:g.4788375A>G	NCBI36
NG_032174.1:g.9578T>C , LRG_455:g.9578T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.532-189T>C MANE Select	ENSP00000322832.6:n.532-189T>C
ENST00000322048.11:c.532-189T>C	ENSP00000322832.5:n.532-189T>C
ENST00000586153.1:c.178-189T>C	ENSP00000464699.1:n.178-189T>C
ENST00000586336.5:n.631-189T>C
ENST00000586504.5:c.312-189T>C
ENST00000587377.5:c.545-189T>C	ENSP00000468343.1:n.545-189T>C
ENST00000587711.5:c.217-189T>C	ENSP00000467459.1:n.217-189T>C
ENST00000587843.5:c.*270-189T>C	ENSP00000465970.1:n.*270-189T>C
ENST00000588201.5:c.*523-189T>C	ENSP00000466529.1:n.*523-189T>C
ENST00000589543.5:n.489-189T>C
ENST00000591292.5:n.1861-189T>C
ENST00000591392.5:c.460-189T>C	ENSP00000467509.1:n.460-189T>C
ENST00000592019.1:c.77-558T>C
NM_024589.2:c.532-189T>C , LRG_455t1:c.532-189T>C	NP_078865.1:n.532-189T>C
NR_046480.1:n.856-189T>C
XM_006720947.2:c.532-189T>C	XP_006721010.1:n.532-189T>C
XM_006720948.2:c.262-189T>C	XP_006721011.1:n.262-189T>C
XM_006720947.4:c.532-189T>C	XP_006721010.1:n.532-189T>C
XM_006720948.4:c.262-189T>C	XP_006721011.1:n.262-189T>C
NM_024589.3:c.532-189T>C MANE Select	NP_078865.1:n.532-189T>C
NR_046480.2:n.539-189T>C