Canonical Allele Identifier: CA2181499510

Gene: RORA

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.61037593A= , CM000677.2:g.61037593A=	GRCh38
NC_000015.9:g.61329792A= , CM000677.1:g.61329792A=	GRCh37
NC_000015.8:g.59117084A=	NCBI36
NG_029246.1:g.196711T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335670.11:c.166+191460T= MANE Select	ENSP00000335087.6:n.166+191460T=
ENST00000335670.10:c.166+191460T=	ENSP00000335087.6:n.166+191460T=
ENST00000551975.5:c.81+191460T=
ENST00000557822.5:n.191+191460T=
ENST00000559145.1:n.173+191460T=
ENST00000561093.1:n.179+191460T=
NM_134261.2:c.166+191460T=	NP_599023.1:n.166+191460T=
XM_011521878.1:c.-328+191460T=	XP_011520180.1:n.-328+191460T=
XM_011521878.2:c.-328+191460T=	XP_011520180.1:n.-328+191460T=
XR_001751773.2:n.2532T=
XR_001751776.2:n.1088+1444T=
XR_001751777.2:n.967-2667T=
XR_002957755.1:n.7557T=
XR_002957756.1:n.4508T=
XR_002957757.1:n.7557T=
XR_002957758.1:n.7557T=
XR_002957759.1:n.7557T=
XR_002957760.1:n.11154T=
XR_002957761.1:n.7557T=
NM_134261.3:c.166+191460T= MANE Select	NP_599023.1:n.166+191460T=