Canonical Allele Identifier: CA2181499514
Gene: RORA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.61037602C= , CM000677.2:g.61037602C= GRCh38
NC_000015.9:g.61329801C= , CM000677.1:g.61329801C= GRCh37
NC_000015.8:g.59117093C= NCBI36
NG_029246.1:g.196702G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000335670.11:c.166+191451G= MANE Select ENSP00000335087.6:n.166+191451G=
ENST00000335670.10:c.166+191451G= ENSP00000335087.6:n.166+191451G=
ENST00000551975.5:c.81+191451G=
ENST00000557822.5:n.191+191451G=
ENST00000559145.1:n.173+191451G=
ENST00000561093.1:n.179+191451G=
NM_134261.2:c.166+191451G= NP_599023.1:n.166+191451G=
XM_011521878.1:c.-328+191451G= XP_011520180.1:n.-328+191451G=
XM_011521878.2:c.-328+191451G= XP_011520180.1:n.-328+191451G=
XR_001751773.2:n.2523G=
XR_001751776.2:n.1088+1435G=
XR_001751777.2:n.967-2676G=
XR_002957755.1:n.7548G=
XR_002957756.1:n.4499G=
XR_002957757.1:n.7548G=
XR_002957758.1:n.7548G=
XR_002957759.1:n.7548G=
XR_002957760.1:n.11145G=
XR_002957761.1:n.7548G=
NM_134261.3:c.166+191451G= MANE Select NP_599023.1:n.166+191451G=