Canonical Allele Identifier: CA2804397064

Gene: RORA

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.60998064C>T , CM000677.2:g.60998064C>T	GRCh38
NC_000015.9:g.61290263C>T , CM000677.1:g.61290263C>T	GRCh37
NC_000015.8:g.59077555C>T	NCBI36
NG_029246.1:g.236240G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335670.11:c.166+230989G>A MANE Select	ENSP00000335087.6:n.166+230989G>A
ENST00000335670.10:c.166+230989G>A	ENSP00000335087.6:n.166+230989G>A
ENST00000551975.5:c.81+230989G>A
ENST00000557822.5:n.191+230989G>A
ENST00000559145.1:n.173+230989G>A
ENST00000561093.1:n.179+230989G>A
NM_134261.2:c.166+230989G>A	NP_599023.1:n.166+230989G>A
XM_011521876.1:c.34+17734G>A	XP_011520178.1:n.34+17734G>A
XM_011521878.1:c.-328+230989G>A	XP_011520180.1:n.-328+230989G>A
XM_011521878.2:c.-328+230989G>A	XP_011520180.1:n.-328+230989G>A
NM_134261.3:c.166+230989G>A MANE Select	NP_599023.1:n.166+230989G>A