Canonical Allele Identifier: CA2181480929

Gene: RORA

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.60998348T= , CM000677.2:g.60998348T=	GRCh38
NC_000015.9:g.61290547T= , CM000677.1:g.61290547T=	GRCh37
NC_000015.8:g.59077839T=	NCBI36
NG_029246.1:g.235956A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335670.11:c.166+230705A= MANE Select	ENSP00000335087.6:n.166+230705A=
ENST00000335670.10:c.166+230705A=	ENSP00000335087.6:n.166+230705A=
ENST00000551975.5:c.81+230705A=
ENST00000557822.5:n.191+230705A=
ENST00000559145.1:n.173+230705A=
ENST00000561093.1:n.179+230705A=
NM_134261.2:c.166+230705A=	NP_599023.1:n.166+230705A=
XM_011521876.1:c.34+17450A=	XP_011520178.1:n.34+17450A=
XM_011521878.1:c.-328+230705A=	XP_011520180.1:n.-328+230705A=
XM_011521878.2:c.-328+230705A=	XP_011520180.1:n.-328+230705A=
NM_134261.3:c.166+230705A= MANE Select	NP_599023.1:n.166+230705A=