Canonical Allele Identifier: CA14184109

Gene: RORA

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.60872000G>A , CM000677.2:g.60872000G>A	GRCh38
NC_000015.9:g.61164199G>A , CM000677.1:g.61164199G>A	GRCh37
NC_000015.8:g.58951491G>A	NCBI36
NG_029246.1:g.362304C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335670.11:c.167-193314C>T MANE Select	ENSP00000335087.6:n.167-193314C>T
ENST00000335670.10:c.167-193314C>T	ENSP00000335087.6:n.167-193314C>T
ENST00000551975.5:c.82-193314C>T
ENST00000557822.5:n.192-193314C>T
ENST00000559145.1:n.174-193314C>T
ENST00000561093.1:n.180-193314C>T
NM_134261.2:c.167-193314C>T	NP_599023.1:n.167-193314C>T
XM_011521876.1:c.34+143798C>T	XP_011520178.1:n.34+143798C>T
XM_011521878.1:c.-327-193314C>T	XP_011520180.1:n.-327-193314C>T
XR_429539.2:n.7080+3750G>A
XR_932322.1:n.7080+3750G>A
XR_932323.1:n.6997-5120G>A
XM_011521878.2:c.-327-193314C>T	XP_011520180.1:n.-327-193314C>T
XR_001751785.1:n.228+3750G>A
NM_134261.3:c.167-193314C>T MANE Select	NP_599023.1:n.167-193314C>T