Canonical Allele Identifier: CA970530567

Gene: RORA

Linked Data

• dbSNP Id: rs2079370100
• gnomAD v3: 15-61148472-CG-C
• gnomAD v4: 15-61148472-CG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.61148473del , CM000677.2:g.61148473del	GRCh38
NC_000015.9:g.61440672del , CM000677.1:g.61440672del	GRCh37
NC_000015.8:g.59227964del	NCBI36
NG_029246.1:g.85831del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335670.11:c.166+80580del MANE Select	ENSP00000335087.6:n.166+80580del
ENST00000335670.10:c.166+80580del	ENSP00000335087.6:n.166+80580del
ENST00000551975.5:c.81+80580del
ENST00000557822.5:n.191+80580del
ENST00000559145.1:n.173+80580del
ENST00000560300.1:n.181+80580del
ENST00000561093.1:n.179+80580del
NM_134261.2:c.166+80580del	NP_599023.1:n.166+80580del
XM_011521878.1:c.-328+80580del	XP_011520180.1:n.-328+80580del
XM_011521878.2:c.-328+80580del	XP_011520180.1:n.-328+80580del
NM_134261.3:c.166+80580del MANE Select	NP_599023.1:n.166+80580del