Canonical Allele Identifier: CA2181411757

Gene: RORA

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.60855305T= , CM000677.2:g.60855305T=	GRCh38
NC_000015.9:g.61147504T= , CM000677.1:g.61147504T=	GRCh37
NC_000015.8:g.58934796T=	NCBI36
NG_029246.1:g.378999A=

Transcript Alleles

HGVS	Amino-acid Change
NM_134261.3:c.167-176619A= MANE Select	NP_599023.1:n.167-176619A=
ENST00000335670.11:c.167-176619A= MANE Select	ENSP00000335087.6:n.167-176619A=
NM_134261.2:c.167-176619A=	NP_599023.1:n.167-176619A=
ENST00000335670.10:c.167-176619A=	ENSP00000335087.6:n.167-176619A=
ENST00000551975.5:c.82-176619A=
ENST00000557822.5:n.192-176619A=
ENST00000559145.1:n.174-176619A=
ENST00000561093.1:n.180-176619A=
XM_011521876.1:c.34+160493A=	XP_011520178.1:n.34+160493A=
XM_011521878.1:c.-327-176619A=	XP_011520180.1:n.-327-176619A=
XM_011521878.2:c.-327-176619A=	XP_011520180.1:n.-327-176619A=