Canonical Allele Identifier: CA2181480874

Gene: RORA

Linked Data

• dbSNP Id: rs1894624161

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.60998227_60998229dup , CM000677.2:g.60998227_60998229dup	GRCh38
NC_000015.9:g.61290426_61290428dup , CM000677.1:g.61290426_61290428dup	GRCh37
NC_000015.8:g.59077718_59077720dup	NCBI36
NG_029246.1:g.236075_236077dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335670.11:c.166+230824_166+230826dup MANE Select	ENSP00000335087.6:n.166+230824_166+230826dup
ENST00000335670.10:c.166+230824_166+230826dup	ENSP00000335087.6:n.166+230824_166+230826dup
ENST00000551975.5:c.81+230824_81+230826dup
ENST00000557822.5:n.191+230824_191+230826dup
ENST00000559145.1:n.173+230824_173+230826dup
ENST00000561093.1:n.179+230824_179+230826dup
NM_134261.2:c.166+230824_166+230826dup	NP_599023.1:n.166+230824_166+230826dup
XM_011521876.1:c.34+17569_34+17571dup	XP_011520178.1:n.34+17569_34+17571dup
XM_011521878.1:c.-328+230824_-328+230826dup	XP_011520180.1:n.-328+230824_-328+230826dup
XM_011521878.2:c.-328+230824_-328+230826dup	XP_011520180.1:n.-328+230824_-328+230826dup
NM_134261.3:c.166+230824_166+230826dup MANE Select	NP_599023.1:n.166+230824_166+230826dup