Canonical Allele Identifier: CA620716817

Gene: ROGDI

Linked Data

• dbSNP Id: rs1567597235
• gnomAD v2: 16-4847874-CCCGGCCCTCCAGGTGTGGAGGGATGGGGTGGGCG-C
• gnomAD v4: 16-4797873-CCCGGCCCTCCAGGTGTGGAGGGATGGGGTGGGCG-C
• MyVariant Identifiers: chr16:g.4847875_4847908del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4797874_4797907del , CM000678.2:g.4797874_4797907del	GRCh38
NC_000016.9:g.4847875_4847908del , CM000678.1:g.4847875_4847908del	GRCh37
NC_000016.8:g.4787876_4787909del	NCBI36
NG_032174.1:g.10044_10077del , LRG_455:g.10044_10077del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.695+31_696-34del MANE Select	ENSP00000322832.6:n.695+31_696-34del
ENST00000322048.11:c.695+31_696-34del	ENSP00000322832.5:n.695+31_696-34del
ENST00000586153.1:c.341+31_342-38del	ENSP00000464699.1:n.341+31_342-38del
ENST00000586336.5:n.794+31_795-34del
ENST00000586504.5:c.426-67_426-34del
ENST00000587377.5:c.*15+31_*16-34del	ENSP00000468343.1:n.*15+31_*16-34del
ENST00000587711.5:c.380+31_381-34del	ENSP00000467459.1:n.380+31_381-34del
ENST00000587843.5:c.*433+31_*434-34del	ENSP00000465970.1:n.*433+31_*434-34del
ENST00000588201.5:c.*686+31_*687-34del	ENSP00000466529.1:n.*686+31_*687-34del
ENST00000589543.5:n.652+31_653-34del
ENST00000591292.5:n.2024+31_2025-34del
ENST00000591392.5:c.623+31_624-34del	ENSP00000467509.1:n.623+31_624-34del
ENST00000592019.1:c.77-92_77-59del
NM_024589.2:c.695+31_696-34del , LRG_455t1:c.695+31_696-34del	NP_078865.1:n.695+31_696-34del
NR_046480.1:n.1019+31_1020-34del
XM_006720947.2:c.695+31_696-13del	XP_006721010.1:n.695+31_696-13del
XM_006720948.2:c.425+31_426-13del	XP_006721011.1:n.425+31_426-13del
XM_006720947.4:c.695+31_696-13del	XP_006721010.1:n.695+31_696-13del
XM_006720948.4:c.425+31_426-13del	XP_006721011.1:n.425+31_426-13del
NM_024589.3:c.695+31_696-34del MANE Select	NP_078865.1:n.695+31_696-34del
NR_046480.2:n.702+31_703-34del