Canonical Allele Identifier: CA2804397068
Gene: RORA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.60998191_60998192insTTTTTTTT , CM000677.2:g.60998191_60998192insTTTTTTTT GRCh38
NC_000015.9:g.61290390_61290391insTTTTTTTT , CM000677.1:g.61290390_61290391insTTTTTTTT GRCh37
NC_000015.8:g.59077682_59077683insTTTTTTTT NCBI36
NG_029246.1:g.236114_236115insAAAAAAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000335670.11:c.166+230863_166+230864insAAAAAAAA MANE Select ENSP00000335087.6:n.166+230863_166+230864insAAAAAAAA
ENST00000335670.10:c.166+230863_166+230864insAAAAAAAA ENSP00000335087.6:n.166+230863_166+230864insAAAAAAAA
ENST00000551975.5:c.81+230863_81+230864insAAAAAAAA
ENST00000557822.5:n.191+230863_191+230864insAAAAAAAA
ENST00000559145.1:n.173+230863_173+230864insAAAAAAAA
ENST00000561093.1:n.179+230863_179+230864insAAAAAAAA
NM_134261.2:c.166+230863_166+230864insAAAAAAAA NP_599023.1:n.166+230863_166+230864insAAAAAAAA
XM_011521876.1:c.34+17608_34+17609insAAAAAAAA XP_011520178.1:n.34+17608_34+17609insAAAAAAAA
XM_011521878.1:c.-328+230863_-328+230864insAAAAAAAA XP_011520180.1:n.-328+230863_-328+230864insAAAAAAAA
XM_011521878.2:c.-328+230863_-328+230864insAAAAAAAA XP_011520180.1:n.-328+230863_-328+230864insAAAAAAAA
NM_134261.3:c.166+230863_166+230864insAAAAAAAA MANE Select NP_599023.1:n.166+230863_166+230864insAAAAAAAA