Canonical Allele Identifier: CA2181474715

Gene: RORA

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.60985277T= , CM000677.2:g.60985277T=	GRCh38
NC_000015.9:g.61277476T= , CM000677.1:g.61277476T=	GRCh37
NC_000015.8:g.59064768T=	NCBI36
NG_029246.1:g.249027A=

Transcript Alleles

HGVS	Amino-acid Change
NM_134261.3:c.166+243776A= MANE Select	NP_599023.1:n.166+243776A=
ENST00000335670.11:c.166+243776A= MANE Select	ENSP00000335087.6:n.166+243776A=
NM_134261.2:c.166+243776A=	NP_599023.1:n.166+243776A=
ENST00000335670.10:c.166+243776A=	ENSP00000335087.6:n.166+243776A=
ENST00000551975.5:c.81+243776A=
ENST00000557822.5:n.191+243776A=
ENST00000559145.1:n.173+243776A=
ENST00000561093.1:n.179+243776A=
XM_011521876.1:c.34+30521A=	XP_011520178.1:n.34+30521A=
XM_011521878.1:c.-328+243776A=	XP_011520180.1:n.-328+243776A=
XM_011521878.2:c.-328+243776A=	XP_011520180.1:n.-328+243776A=