Canonical Allele Identifier: CA2804397067

Gene: RORA

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.60998182_60998189del , CM000677.2:g.60998182_60998189del	GRCh38
NC_000015.9:g.61290381_61290388del , CM000677.1:g.61290381_61290388del	GRCh37
NC_000015.8:g.59077673_59077680del	NCBI36
NG_029246.1:g.236115_236122del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335670.11:c.166+230864_166+230871del MANE Select	ENSP00000335087.6:n.166+230864_166+230871del
ENST00000335670.10:c.166+230864_166+230871del	ENSP00000335087.6:n.166+230864_166+230871del
ENST00000551975.5:c.81+230864_81+230871del
ENST00000557822.5:n.191+230864_191+230871del
ENST00000559145.1:n.173+230864_173+230871del
ENST00000561093.1:n.179+230864_179+230871del
NM_134261.2:c.166+230864_166+230871del	NP_599023.1:n.166+230864_166+230871del
XM_011521876.1:c.34+17609_34+17616del	XP_011520178.1:n.34+17609_34+17616del
XM_011521878.1:c.-328+230864_-328+230871del	XP_011520180.1:n.-328+230864_-328+230871del
XM_011521878.2:c.-328+230864_-328+230871del	XP_011520180.1:n.-328+230864_-328+230871del
NM_134261.3:c.166+230864_166+230871del MANE Select	NP_599023.1:n.166+230864_166+230871del