Canonical Allele Identifier: CA2181524685

Gene: RORA

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.61089054G= , CM000677.2:g.61089054G=	GRCh38
NC_000015.9:g.61381253G= , CM000677.1:g.61381253G=	GRCh37
NC_000015.8:g.59168545G=	NCBI36
NG_029246.1:g.145250C=

Transcript Alleles

HGVS	Amino-acid Change
NM_134261.3:c.166+139999C= MANE Select	NP_599023.1:n.166+139999C=
ENST00000335670.11:c.166+139999C= MANE Select	ENSP00000335087.6:n.166+139999C=
NM_134261.2:c.166+139999C=	NP_599023.1:n.166+139999C=
ENST00000335670.10:c.166+139999C=	ENSP00000335087.6:n.166+139999C=
ENST00000551975.5:c.81+139999C=
ENST00000557822.5:n.191+139999C=
ENST00000559145.1:n.173+139999C=
ENST00000560300.1:n.182-47920C=
ENST00000561093.1:n.179+139999C=
XM_011521878.1:c.-328+139999C=	XP_011520180.1:n.-328+139999C=
XM_011521878.2:c.-328+139999C=	XP_011520180.1:n.-328+139999C=
XR_001751773.2:n.966+5302C=
XR_001751776.2:n.966+5302C=
XR_001751777.2:n.966+5302C=
XR_002957756.1:n.966+5302C=
XR_002957760.1:n.7612+5302C=