Canonical Allele Identifier: CA2181553229

Gene: RORA

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.61148472C= , CM000677.2:g.61148472C=	GRCh38
NC_000015.9:g.61440671C= , CM000677.1:g.61440671C=	GRCh37
NC_000015.8:g.59227963C=	NCBI36
NG_029246.1:g.85832G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000335670.11:c.166+80581G= MANE Select	ENSP00000335087.6:n.166+80581G=
ENST00000335670.10:c.166+80581G=	ENSP00000335087.6:n.166+80581G=
ENST00000551975.5:c.81+80581G=
ENST00000557822.5:n.191+80581G=
ENST00000559145.1:n.173+80581G=
ENST00000560300.1:n.181+80581G=
ENST00000561093.1:n.179+80581G=
NM_134261.2:c.166+80581G=	NP_599023.1:n.166+80581G=
XM_011521878.1:c.-328+80581G=	XP_011520180.1:n.-328+80581G=
XM_011521878.2:c.-328+80581G=	XP_011520180.1:n.-328+80581G=
NM_134261.3:c.166+80581G= MANE Select	NP_599023.1:n.166+80581G=