Canonical Allele Identifier: CA970507589

Gene: RORA

Linked Data

• dbSNP Id: rs1894621182
• gnomAD v3: 15-60998166-ATCTT-A
• gnomAD v4: 15-60998166-ATCTT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.60998172_60998175del , CM000677.2:g.60998172_60998175del	GRCh38
NC_000015.9:g.61290371_61290374del , CM000677.1:g.61290371_61290374del	GRCh37
NC_000015.8:g.59077663_59077666del	NCBI36
NG_029246.1:g.236134_236137del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335670.11:c.166+230883_166+230886del MANE Select	ENSP00000335087.6:n.166+230883_166+230886del
ENST00000335670.10:c.166+230883_166+230886del	ENSP00000335087.6:n.166+230883_166+230886del
ENST00000551975.5:c.81+230883_81+230886del
ENST00000557822.5:n.191+230883_191+230886del
ENST00000559145.1:n.173+230883_173+230886del
ENST00000561093.1:n.179+230883_179+230886del
NM_134261.2:c.166+230883_166+230886del	NP_599023.1:n.166+230883_166+230886del
XM_011521876.1:c.34+17628_34+17631del	XP_011520178.1:n.34+17628_34+17631del
XM_011521878.1:c.-328+230883_-328+230886del	XP_011520180.1:n.-328+230883_-328+230886del
XM_011521878.2:c.-328+230883_-328+230886del	XP_011520180.1:n.-328+230883_-328+230886del
NM_134261.3:c.166+230883_166+230886del MANE Select	NP_599023.1:n.166+230883_166+230886del