Canonical Allele Identifier: CA2579753899

Gene: RORA

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.60997989C>A , CM000677.2:g.60997989C>A	GRCh38
NC_000015.9:g.61290188C>A , CM000677.1:g.61290188C>A	GRCh37
NC_000015.8:g.59077480C>A	NCBI36
NG_029246.1:g.236315G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000335670.11:c.166+231064G>T MANE Select	ENSP00000335087.6:n.166+231064G>T
ENST00000335670.10:c.166+231064G>T	ENSP00000335087.6:n.166+231064G>T
ENST00000551975.5:c.81+231064G>T
ENST00000557822.5:n.191+231064G>T
ENST00000559145.1:n.173+231064G>T
ENST00000561093.1:n.179+231064G>T
NM_134261.2:c.166+231064G>T	NP_599023.1:n.166+231064G>T
XM_011521876.1:c.34+17809G>T	XP_011520178.1:n.34+17809G>T
XM_011521878.1:c.-328+231064G>T	XP_011520180.1:n.-328+231064G>T
XM_011521878.2:c.-328+231064G>T	XP_011520180.1:n.-328+231064G>T
NM_134261.3:c.166+231064G>T MANE Select	NP_599023.1:n.166+231064G>T