Canonical Allele Identifier: CA2181371859

Gene: RORA

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.60772552A>T , CM000677.2:g.60772552A>T	GRCh38
NC_000015.9:g.61064751A>T , CM000677.1:g.61064751A>T	GRCh37
NC_000015.8:g.58852043A>T	NCBI36
NG_029246.1:g.461752T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335670.11:c.167-93866T>A MANE Select	ENSP00000335087.6:n.167-93866T>A
ENST00000335670.10:c.167-93866T>A	ENSP00000335087.6:n.167-93866T>A
ENST00000551975.5:c.82-93866T>A
ENST00000557822.5:n.192-93866T>A
ENST00000559145.1:n.174-93866T>A
ENST00000561093.1:n.180-93866T>A
NM_134261.2:c.167-93866T>A	NP_599023.1:n.167-93866T>A
XM_005254584.3:c.28+68518T>A	XP_005254641.1:n.28+68518T>A
XM_011521876.1:c.35-93866T>A	XP_011520178.1:n.35-93866T>A
XM_011521878.1:c.-327-93866T>A	XP_011520180.1:n.-327-93866T>A
XM_005254584.5:c.28+68518T>A	XP_005254641.1:n.28+68518T>A
XM_011521878.2:c.-327-93866T>A	XP_011520180.1:n.-327-93866T>A
NM_134261.3:c.167-93866T>A MANE Select	NP_599023.1:n.167-93866T>A