Canonical Allele Identifier: CA2181499516
Gene: RORA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.61037604T= , CM000677.2:g.61037604T= GRCh38
NC_000015.9:g.61329803T= , CM000677.1:g.61329803T= GRCh37
NC_000015.8:g.59117095T= NCBI36
NG_029246.1:g.196700A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000335670.11:c.166+191449A= MANE Select ENSP00000335087.6:n.166+191449A=
ENST00000335670.10:c.166+191449A= ENSP00000335087.6:n.166+191449A=
ENST00000551975.5:c.81+191449A=
ENST00000557822.5:n.191+191449A=
ENST00000559145.1:n.173+191449A=
ENST00000561093.1:n.179+191449A=
NM_134261.2:c.166+191449A= NP_599023.1:n.166+191449A=
XM_011521878.1:c.-328+191449A= XP_011520180.1:n.-328+191449A=
XM_011521878.2:c.-328+191449A= XP_011520180.1:n.-328+191449A=
XR_001751773.2:n.2521A=
XR_001751776.2:n.1088+1433A=
XR_001751777.2:n.967-2678A=
XR_002957755.1:n.7546A=
XR_002957756.1:n.4497A=
XR_002957757.1:n.7546A=
XR_002957758.1:n.7546A=
XR_002957759.1:n.7546A=
XR_002957760.1:n.11143A=
XR_002957761.1:n.7546A=
NM_134261.3:c.166+191449A= MANE Select NP_599023.1:n.166+191449A=