Canonical Allele Identifier: CA2181371057

Gene: RORA

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.60770839T= , CM000677.2:g.60770839T=	GRCh38
NC_000015.9:g.61063038T= , CM000677.1:g.61063038T=	GRCh37
NC_000015.8:g.58850330T=	NCBI36
NG_029246.1:g.463465A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335670.11:c.167-92153A= MANE Select	ENSP00000335087.6:n.167-92153A=
ENST00000335670.10:c.167-92153A=	ENSP00000335087.6:n.167-92153A=
ENST00000551975.5:c.82-92153A=
ENST00000557822.5:n.192-92153A=
ENST00000559145.1:n.174-92153A=
ENST00000561093.1:n.180-92153A=
NM_134261.2:c.167-92153A=	NP_599023.1:n.167-92153A=
XM_005254584.3:c.28+70231A=	XP_005254641.1:n.28+70231A=
XM_011521876.1:c.35-92153A=	XP_011520178.1:n.35-92153A=
XM_011521878.1:c.-327-92153A=	XP_011520180.1:n.-327-92153A=
XM_005254584.5:c.28+70231A=	XP_005254641.1:n.28+70231A=
XM_011521878.2:c.-327-92153A=	XP_011520180.1:n.-327-92153A=
NM_134261.3:c.167-92153A= MANE Select	NP_599023.1:n.167-92153A=