Canonical Allele Identifier: CA2181499554

Gene: RORA

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.61037686G= , CM000677.2:g.61037686G=	GRCh38
NC_000015.9:g.61329885G= , CM000677.1:g.61329885G=	GRCh37
NC_000015.8:g.59117177G=	NCBI36
NG_029246.1:g.196618C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335670.11:c.166+191367C= MANE Select	ENSP00000335087.6:n.166+191367C=
ENST00000335670.10:c.166+191367C=	ENSP00000335087.6:n.166+191367C=
ENST00000551975.5:c.81+191367C=
ENST00000557822.5:n.191+191367C=
ENST00000559145.1:n.173+191367C=
ENST00000561093.1:n.179+191367C=
NM_134261.2:c.166+191367C=	NP_599023.1:n.166+191367C=
XM_011521878.1:c.-328+191367C=	XP_011520180.1:n.-328+191367C=
XM_011521878.2:c.-328+191367C=	XP_011520180.1:n.-328+191367C=
XR_001751773.2:n.2439C=
XR_001751776.2:n.1088+1351C=
XR_001751777.2:n.967-2760C=
XR_002957755.1:n.7464C=
XR_002957756.1:n.4415C=
XR_002957757.1:n.7464C=
XR_002957758.1:n.7464C=
XR_002957759.1:n.7464C=
XR_002957760.1:n.11061C=
XR_002957761.1:n.7464C=
NM_134261.3:c.166+191367C= MANE Select	NP_599023.1:n.166+191367C=