Canonical Allele Identifier: CA2181537692

Gene: RORA

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.61116504G= , CM000677.2:g.61116504G=	GRCh38
NC_000015.9:g.61408703G= , CM000677.1:g.61408703G=	GRCh37
NC_000015.8:g.59195995G=	NCBI36
NG_029246.1:g.117800C=

Transcript Alleles

HGVS	Amino-acid Change
NM_134261.3:c.166+112549C= MANE Select	NP_599023.1:n.166+112549C=
ENST00000335670.11:c.166+112549C= MANE Select	ENSP00000335087.6:n.166+112549C=
NM_134261.2:c.166+112549C=	NP_599023.1:n.166+112549C=
ENST00000335670.10:c.166+112549C=	ENSP00000335087.6:n.166+112549C=
ENST00000551975.5:c.81+112549C=
ENST00000557822.5:n.191+112549C=
ENST00000559145.1:n.173+112549C=
ENST00000560300.1:n.182-75370C=
ENST00000561093.1:n.179+112549C=
XM_011521878.1:c.-328+112549C=	XP_011520180.1:n.-328+112549C=
XM_011521878.2:c.-328+112549C=	XP_011520180.1:n.-328+112549C=
XR_002957760.1:n.2765C=