Canonical Allele Identifier: CA394654974

Gene: ROGDI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4801322C>G , CM000678.2:g.4801322C>G	GRCh38
NC_000016.9:g.4851323C>G , CM000678.1:g.4851323C>G	GRCh37
NC_000016.8:g.4791324C>G	NCBI36
NG_032174.1:g.6629G>C , LRG_455:g.6629G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_024589.3:c.201-1G>C MANE Select	NP_078865.1:n.201-1G>C
ENST00000322048.12:c.201-1G>C MANE Select	ENSP00000322832.6:n.201-1G>C
NM_024589.2:c.201-1G>C , LRG_455t1:c.201-1G>C	NP_078865.1:n.201-1G>C
NR_046480.1:n.579+181G>C
NR_046480.2:n.262+181G>C
ENST00000322048.11:c.201-1G>C	ENSP00000322832.5:n.201-1G>C
ENST00000585653.1:n.333-1G>C
ENST00000585871.1:n.690G>C
ENST00000586336.5:n.354+181G>C
ENST00000587377.5:c.201-1G>C	ENSP00000468343.1:n.201-1G>C
ENST00000587711.5:c.117+1060G>C	ENSP00000467459.1:n.117+1060G>C
ENST00000587843.5:c.200+181G>C	ENSP00000465970.1:n.200+181G>C
ENST00000588201.5:c.201-1G>C	ENSP00000466529.1:n.201-1G>C
ENST00000589543.5:n.158-1G>C
ENST00000591292.5:n.841G>C
ENST00000591392.5:c.129-1G>C	ENSP00000467509.1:n.129-1G>C
XM_006720947.2:c.201-1G>C	XP_006721010.1:n.201-1G>C
XM_006720947.4:c.201-1G>C	XP_006721010.1:n.201-1G>C
XM_006720948.2:c.-16+181G>C	XP_006721011.1:n.-16+181G>C
XM_006720948.4:c.-16+181G>C	XP_006721011.1:n.-16+181G>C