Canonical Allele Identifier: CA2521249619
Gene: RORA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.60998012_60998013insAAATGTGGGTTTC , CM000677.2:g.60998012_60998013insAAATGTGGGTTTC GRCh38
NC_000015.9:g.61290211_61290212insAAATGTGGGTTTC , CM000677.1:g.61290211_61290212insAAATGTGGGTTTC GRCh37
NC_000015.8:g.59077503_59077504insAAATGTGGGTTTC NCBI36
NG_029246.1:g.236291_236292insGAAACCCACATTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000335670.11:c.166+231040_166+231041insGAAACCCACATTT MANE Select ENSP00000335087.6:n.166+231040_166+231041insGAAACCCACATTT
ENST00000335670.10:c.166+231040_166+231041insGAAACCCACATTT ENSP00000335087.6:n.166+231040_166+231041insGAAACCCACATTT
ENST00000551975.5:c.81+231040_81+231041insGAAACCCACATTT
ENST00000557822.5:n.191+231040_191+231041insGAAACCCACATTT
ENST00000559145.1:n.173+231040_173+231041insGAAACCCACATTT
ENST00000561093.1:n.179+231040_179+231041insGAAACCCACATTT
NM_134261.2:c.166+231040_166+231041insGAAACCCACATTT NP_599023.1:n.166+231040_166+231041insGAAACCCACATTT
XM_011521876.1:c.34+17785_34+17786insGAAACCCACATTT XP_011520178.1:n.34+17785_34+17786insGAAACCCACATTT
XM_011521878.1:c.-328+231040_-328+231041insGAAACCCACATTT XP_011520180.1:n.-328+231040_-328+231041insGAAACCCACATTT
XM_011521878.2:c.-328+231040_-328+231041insGAAACCCACATTT XP_011520180.1:n.-328+231040_-328+231041insGAAACCCACATTT
NM_134261.3:c.166+231040_166+231041insGAAACCCACATTT MANE Select NP_599023.1:n.166+231040_166+231041insGAAACCCACATTT