Canonical Allele Identifier: CA2838532197

Gene: RORA

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.61045893A>G , CM000677.2:g.61045893A>G	GRCh38
NC_000015.9:g.61338092A>G , CM000677.1:g.61338092A>G	GRCh37
NC_000015.8:g.59125384A>G	NCBI36
NG_029246.1:g.188411T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335670.11:c.166+183160T>C MANE Select	ENSP00000335087.6:n.166+183160T>C
ENST00000335670.10:c.166+183160T>C	ENSP00000335087.6:n.166+183160T>C
ENST00000551975.5:c.81+183160T>C
ENST00000557822.5:n.191+183160T>C
ENST00000559145.1:n.173+183160T>C
ENST00000560300.1:n.182-4759T>C
ENST00000561093.1:n.179+183160T>C
NM_134261.2:c.166+183160T>C	NP_599023.1:n.166+183160T>C
XM_011521878.1:c.-328+183160T>C	XP_011520180.1:n.-328+183160T>C
XM_011521878.2:c.-328+183160T>C	XP_011520180.1:n.-328+183160T>C
XR_001751773.2:n.967-4759T>C
XR_001751776.2:n.967-4759T>C
XR_001751777.2:n.967-10967T>C
XR_002957756.1:n.967-4759T>C
XR_002957760.1:n.7613-4759T>C
NM_134261.3:c.166+183160T>C MANE Select	NP_599023.1:n.166+183160T>C