Canonical Allele Identifier: CA2804394772

Gene: RORA

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.60901981G>A , CM000677.2:g.60901981G>A	GRCh38
NC_000015.9:g.61194180G>A , CM000677.1:g.61194180G>A	GRCh37
NC_000015.8:g.58981472G>A	NCBI36
NG_029246.1:g.332323C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335670.11:c.167-223295C>T MANE Select	ENSP00000335087.6:n.167-223295C>T
ENST00000335670.10:c.167-223295C>T	ENSP00000335087.6:n.167-223295C>T
ENST00000551975.5:c.82-223295C>T
ENST00000557822.5:n.192-223295C>T
ENST00000559145.1:n.174-223295C>T
ENST00000561093.1:n.180-223295C>T
NM_134261.2:c.167-223295C>T	NP_599023.1:n.167-223295C>T
XM_011521876.1:c.34+113817C>T	XP_011520178.1:n.34+113817C>T
XM_011521878.1:c.-327-223295C>T	XP_011520180.1:n.-327-223295C>T
XM_011521878.2:c.-327-223295C>T	XP_011520180.1:n.-327-223295C>T
NM_134261.3:c.167-223295C>T MANE Select	NP_599023.1:n.167-223295C>T