Canonical Allele Identifier: CA2181434236

Gene: RORA

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.60902035A= , CM000677.2:g.60902035A=	GRCh38
NC_000015.9:g.61194234A= , CM000677.1:g.61194234A=	GRCh37
NC_000015.8:g.58981526A=	NCBI36
NG_029246.1:g.332269T=

Transcript Alleles

HGVS	Amino-acid Change
NM_134261.3:c.167-223349T= MANE Select	NP_599023.1:n.167-223349T=
ENST00000335670.11:c.167-223349T= MANE Select	ENSP00000335087.6:n.167-223349T=
NM_134261.2:c.167-223349T=	NP_599023.1:n.167-223349T=
ENST00000335670.10:c.167-223349T=	ENSP00000335087.6:n.167-223349T=
ENST00000551975.5:c.82-223349T=
ENST00000557822.5:n.192-223349T=
ENST00000559145.1:n.174-223349T=
ENST00000561093.1:n.180-223349T=
XM_011521876.1:c.34+113763T=	XP_011520178.1:n.34+113763T=
XM_011521878.1:c.-327-223349T=	XP_011520180.1:n.-327-223349T=
XM_011521878.2:c.-327-223349T=	XP_011520180.1:n.-327-223349T=