Canonical Allele Identifier: CA14161284

Gene: RORA

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.61044243C>G , CM000677.2:g.61044243C>G	GRCh38
NC_000015.9:g.61336442C>G , CM000677.1:g.61336442C>G	GRCh37
NC_000015.8:g.59123734C>G	NCBI36
NG_029246.1:g.190061G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335670.11:c.166+184810G>C MANE Select	ENSP00000335087.6:n.166+184810G>C
ENST00000335670.10:c.166+184810G>C	ENSP00000335087.6:n.166+184810G>C
ENST00000551975.5:c.81+184810G>C
ENST00000557822.5:n.191+184810G>C
ENST00000559145.1:n.173+184810G>C
ENST00000560300.1:n.182-3109G>C
ENST00000561093.1:n.179+184810G>C
NM_134261.2:c.166+184810G>C	NP_599023.1:n.166+184810G>C
XM_011521878.1:c.-328+184810G>C	XP_011520180.1:n.-328+184810G>C
XM_011521878.2:c.-328+184810G>C	XP_011520180.1:n.-328+184810G>C
XR_001751773.2:n.967-3109G>C
XR_001751776.2:n.967-3109G>C
XR_001751777.2:n.967-9317G>C
XR_002957755.1:n.907G>C
XR_002957756.1:n.967-3109G>C
XR_002957757.1:n.907G>C
XR_002957758.1:n.907G>C
XR_002957759.1:n.907G>C
XR_002957760.1:n.7613-3109G>C
XR_002957761.1:n.907G>C
NM_134261.3:c.166+184810G>C MANE Select	NP_599023.1:n.166+184810G>C