Canonical Allele Identifier: CA2181480771

Gene: RORA

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.60997993G= , CM000677.2:g.60997993G=	GRCh38
NC_000015.9:g.61290192G= , CM000677.1:g.61290192G=	GRCh37
NC_000015.8:g.59077484G=	NCBI36
NG_029246.1:g.236311C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335670.11:c.166+231060C= MANE Select	ENSP00000335087.6:n.166+231060C=
ENST00000335670.10:c.166+231060C=	ENSP00000335087.6:n.166+231060C=
ENST00000551975.5:c.81+231060C=
ENST00000557822.5:n.191+231060C=
ENST00000559145.1:n.173+231060C=
ENST00000561093.1:n.179+231060C=
NM_134261.2:c.166+231060C=	NP_599023.1:n.166+231060C=
XM_011521876.1:c.34+17805C=	XP_011520178.1:n.34+17805C=
XM_011521878.1:c.-328+231060C=	XP_011520180.1:n.-328+231060C=
XM_011521878.2:c.-328+231060C=	XP_011520180.1:n.-328+231060C=
NM_134261.3:c.166+231060C= MANE Select	NP_599023.1:n.166+231060C=