Canonical Allele Identifier: CA2181572231

Gene: RORA

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.61188522C= , CM000677.2:g.61188522C=	GRCh38
NC_000015.9:g.61480721C= , CM000677.1:g.61480721C=	GRCh37
NC_000015.8:g.59268013C=	NCBI36
NG_029246.1:g.45782G=

Transcript Alleles

HGVS	Amino-acid Change
NM_134261.3:c.166+40531G= MANE Select	NP_599023.1:n.166+40531G=
ENST00000335670.11:c.166+40531G= MANE Select	ENSP00000335087.6:n.166+40531G=
NM_134261.2:c.166+40531G=	NP_599023.1:n.166+40531G=
ENST00000335670.10:c.166+40531G=	ENSP00000335087.6:n.166+40531G=
ENST00000551975.5:c.81+40531G=
ENST00000557822.5:n.191+40531G=
ENST00000558904.2:c.104-12066G=	ENSP00000484955.1:n.104-12066G=
ENST00000559145.1:n.173+40531G=
ENST00000560300.1:n.181+40531G=
ENST00000561093.1:n.179+40531G=
XM_011521878.1:c.-328+40531G=	XP_011520180.1:n.-328+40531G=
XM_011521878.2:c.-328+40531G=	XP_011520180.1:n.-328+40531G=
XR_429538.2:n.415+5440C=
XR_932316.1:n.415+5440C=
XR_932317.1:n.414+5440C=
XR_932318.1:n.418+5440C=
XR_932319.1:n.624+5440C=
XR_932320.1:n.411+5440C=