Canonical Allele Identifier: CA2181499527
Gene: RORA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.61037632A= , CM000677.2:g.61037632A= GRCh38
NC_000015.9:g.61329831A= , CM000677.1:g.61329831A= GRCh37
NC_000015.8:g.59117123A= NCBI36
NG_029246.1:g.196672T=

Transcript Alleles

HGVS Amino-acid change
ENST00000335670.11:c.166+191421T= MANE Select ENSP00000335087.6:n.166+191421T=
ENST00000335670.10:c.166+191421T= ENSP00000335087.6:n.166+191421T=
ENST00000551975.5:c.81+191421T=
ENST00000557822.5:n.191+191421T=
ENST00000559145.1:n.173+191421T=
ENST00000561093.1:n.179+191421T=
NM_134261.2:c.166+191421T= NP_599023.1:n.166+191421T=
XM_011521878.1:c.-328+191421T= XP_011520180.1:n.-328+191421T=
XM_011521878.2:c.-328+191421T= XP_011520180.1:n.-328+191421T=
XR_001751773.2:n.2493T=
XR_001751776.2:n.1088+1405T=
XR_001751777.2:n.967-2706T=
XR_002957755.1:n.7518T=
XR_002957756.1:n.4469T=
XR_002957757.1:n.7518T=
XR_002957758.1:n.7518T=
XR_002957759.1:n.7518T=
XR_002957760.1:n.11115T=
XR_002957761.1:n.7518T=
NM_134261.3:c.166+191421T= MANE Select NP_599023.1:n.166+191421T=