Canonical Allele Identifier: CA7882430

Gene: ROGDI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4797516G>A , CM000678.2:g.4797516G>A	GRCh38
NC_000016.9:g.4847517G>A , CM000678.1:g.4847517G>A	GRCh37
NC_000016.8:g.4787518G>A	NCBI36
NG_032174.1:g.10435C>T , LRG_455:g.10435C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_024589.3:c.823-15C>T MANE Select	NP_078865.1:n.823-15C>T
ENST00000322048.12:c.823-15C>T MANE Select	ENSP00000322832.6:n.823-15C>T
NM_024589.2:c.823-15C>T , LRG_455t1:c.823-15C>T	NP_078865.1:n.823-15C>T
NR_046480.1:n.1147-15C>T
NR_046480.2:n.830-15C>T
ENST00000322048.11:c.823-15C>T	ENSP00000322832.5:n.823-15C>T
ENST00000586504.5:c.553-15C>T
ENST00000587377.5:c.*143-15C>T	ENSP00000468343.1:n.*143-15C>T
ENST00000587843.5:c.*561-15C>T	ENSP00000465970.1:n.*561-15C>T
ENST00000588201.5:c.*814-15C>T	ENSP00000466529.1:n.*814-15C>T
ENST00000591292.5:n.2152-15C>T
ENST00000592019.1:c.179-15C>T
XM_006720947.2:c.844-15C>T	XP_006721010.1:n.844-15C>T
XM_006720947.4:c.844-15C>T	XP_006721010.1:n.844-15C>T
XM_006720948.2:c.574-15C>T	XP_006721011.1:n.574-15C>T
XM_006720948.4:c.574-15C>T	XP_006721011.1:n.574-15C>T