Canonical Allele Identifier: CA272215335
Gene: RORA HGNC NCBI

Linked Data

dbSNP Id: rs773337015

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.60997845del , CM000677.2:g.60997845del GRCh38
NC_000015.9:g.61290044del , CM000677.1:g.61290044del GRCh37
NC_000015.8:g.59077336del NCBI36
NG_029246.1:g.236459del

Transcript Alleles

HGVS Amino-acid Change
ENST00000335670.11:c.166+231208del MANE Select ENSP00000335087.6:n.166+231208del
ENST00000335670.10:c.166+231208del ENSP00000335087.6:n.166+231208del
ENST00000551975.5:c.81+231208del
ENST00000557822.5:n.191+231208del
ENST00000559145.1:n.173+231208del
ENST00000561093.1:n.179+231208del
NM_134261.2:c.166+231208del NP_599023.1:n.166+231208del
XM_011521876.1:c.34+17953del XP_011520178.1:n.34+17953del
XM_011521878.1:c.-328+231208del XP_011520180.1:n.-328+231208del
XM_011521878.2:c.-328+231208del XP_011520180.1:n.-328+231208del
NM_134261.3:c.166+231208del MANE Select NP_599023.1:n.166+231208del