Canonical Allele Identifier: CA14171345

Gene: RORA

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.60775749C>T , CM000677.2:g.60775749C>T	GRCh38
NC_000015.9:g.61067948C>T , CM000677.1:g.61067948C>T	GRCh37
NC_000015.8:g.58855240C>T	NCBI36
NG_029246.1:g.458555G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335670.11:c.167-97063G>A MANE Select	ENSP00000335087.6:n.167-97063G>A
ENST00000335670.10:c.167-97063G>A	ENSP00000335087.6:n.167-97063G>A
ENST00000551975.5:c.82-97063G>A
ENST00000557822.5:n.192-97063G>A
ENST00000559145.1:n.174-97063G>A
ENST00000561093.1:n.180-97063G>A
NM_134261.2:c.167-97063G>A	NP_599023.1:n.167-97063G>A
XM_005254584.3:c.28+65321G>A	XP_005254641.1:n.28+65321G>A
XM_011521876.1:c.35-97063G>A	XP_011520178.1:n.35-97063G>A
XM_011521878.1:c.-327-97063G>A	XP_011520180.1:n.-327-97063G>A
XM_005254584.5:c.28+65321G>A	XP_005254641.1:n.28+65321G>A
XM_011521878.2:c.-327-97063G>A	XP_011520180.1:n.-327-97063G>A
NM_134261.3:c.167-97063G>A MANE Select	NP_599023.1:n.167-97063G>A