Canonical Allele Identifier: CA2631549966

Gene: ROGDI

Linked Data

• gnomAD v4: 16-4797851-TGA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4797855_4797856del , CM000678.2:g.4797855_4797856del	GRCh38
NC_000016.9:g.4847856_4847857del , CM000678.1:g.4847856_4847857del	GRCh37
NC_000016.8:g.4787857_4787858del	NCBI36
NG_032174.1:g.10098_10099del , LRG_455:g.10098_10099del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.696-13_696-12del MANE Select	ENSP00000322832.6:n.696-13_696-12del
ENST00000322048.11:c.696-13_696-12del	ENSP00000322832.5:n.696-13_696-12del
ENST00000586153.1:c.342-17_342-16del	ENSP00000464699.1:n.342-17_342-16del
ENST00000586336.5:n.795-13_795-12del
ENST00000586504.5:c.426-13_426-12del
ENST00000587377.5:c.*16-13_*16-12del	ENSP00000468343.1:n.*16-13_*16-12del
ENST00000587711.5:c.381-13_381-12del	ENSP00000467459.1:n.381-13_381-12del
ENST00000587843.5:c.*434-13_*434-12del	ENSP00000465970.1:n.*434-13_*434-12del
ENST00000588201.5:c.*687-13_*687-12del	ENSP00000466529.1:n.*687-13_*687-12del
ENST00000589543.5:n.653-13_653-12del
ENST00000591292.5:n.2025-13_2025-12del
ENST00000591392.5:c.624-13_624-12del	ENSP00000467509.1:n.624-13_624-12del
ENST00000592019.1:c.77-38_77-37del
NM_024589.2:c.696-13_696-12del , LRG_455t1:c.696-13_696-12del	NP_078865.1:n.696-13_696-12del
NR_046480.1:n.1020-13_1020-12del
XM_006720947.2:c.704_705del	XP_006721010.1:p.Leu235HisfsTer?
XM_006720948.2:c.434_435del	XP_006721011.1:p.Leu145HisfsTer?
XM_006720947.4:c.704_705del	XP_006721010.1:p.Leu235HisfsTer?
XM_006720948.4:c.434_435del	XP_006721011.1:p.Leu145HisfsTer?
NM_024589.3:c.696-13_696-12del MANE Select	NP_078865.1:n.696-13_696-12del
NR_046480.2:n.703-13_703-12del