Canonical Allele Identifier: CA919568899

Gene: RORA

Linked Data

• dbSNP Id: rs1396129877

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.60998337del , CM000677.2:g.60998337del	GRCh38
NC_000015.9:g.61290536del , CM000677.1:g.61290536del	GRCh37
NC_000015.8:g.59077828del	NCBI36
NG_029246.1:g.235972del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335670.11:c.166+230721del MANE Select	ENSP00000335087.6:n.166+230721del
ENST00000335670.10:c.166+230721del	ENSP00000335087.6:n.166+230721del
ENST00000551975.5:c.81+230721del
ENST00000557822.5:n.191+230721del
ENST00000559145.1:n.173+230721del
ENST00000561093.1:n.179+230721del
NM_134261.2:c.166+230721del	NP_599023.1:n.166+230721del
XM_011521876.1:c.34+17466del	XP_011520178.1:n.34+17466del
XM_011521878.1:c.-328+230721del	XP_011520180.1:n.-328+230721del
XM_011521878.2:c.-328+230721del	XP_011520180.1:n.-328+230721del
NM_134261.3:c.166+230721del MANE Select	NP_599023.1:n.166+230721del