Canonical Allele Identifier: CA2181480921

Gene: RORA

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.60998331_60998332delinsCT , CM000677.2:g.60998331_60998332delinsCT	GRCh38
NC_000015.9:g.61290530_61290531delinsCT , CM000677.1:g.61290530_61290531delinsCT	GRCh37
NC_000015.8:g.59077822_59077823delinsCT	NCBI36
NG_029246.1:g.235972_235973delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335670.11:c.166+230721_166+230722delinsAG MANE Select	ENSP00000335087.6:n.166+230721_166+230722delinsAG
ENST00000335670.10:c.166+230721_166+230722delinsAG	ENSP00000335087.6:n.166+230721_166+230722delinsAG
ENST00000551975.5:c.81+230721_81+230722delinsAG
ENST00000557822.5:n.191+230721_191+230722delinsAG
ENST00000559145.1:n.173+230721_173+230722delinsAG
ENST00000561093.1:n.179+230721_179+230722delinsAG
NM_134261.2:c.166+230721_166+230722delinsAG	NP_599023.1:n.166+230721_166+230722delinsAG
XM_011521876.1:c.34+17466_34+17467delinsAG	XP_011520178.1:n.34+17466_34+17467delinsAG
XM_011521878.1:c.-328+230721_-328+230722delinsAG	XP_011520180.1:n.-328+230721_-328+230722delinsAG
XM_011521878.2:c.-328+230721_-328+230722delinsAG	XP_011520180.1:n.-328+230721_-328+230722delinsAG
NM_134261.3:c.166+230721_166+230722delinsAG MANE Select	NP_599023.1:n.166+230721_166+230722delinsAG