Canonical Allele Identifier: CA2181419739

Gene: RORA

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.60872000G= , CM000677.2:g.60872000G=	GRCh38
NC_000015.9:g.61164199G= , CM000677.1:g.61164199G=	GRCh37
NC_000015.8:g.58951491G=	NCBI36
NG_029246.1:g.362304C=

Transcript Alleles

HGVS	Amino-acid Change
NM_134261.3:c.167-193314C= MANE Select	NP_599023.1:n.167-193314C=
ENST00000335670.11:c.167-193314C= MANE Select	ENSP00000335087.6:n.167-193314C=
NM_134261.2:c.167-193314C=	NP_599023.1:n.167-193314C=
ENST00000335670.10:c.167-193314C=	ENSP00000335087.6:n.167-193314C=
ENST00000551975.5:c.82-193314C=
ENST00000557822.5:n.192-193314C=
ENST00000559145.1:n.174-193314C=
ENST00000561093.1:n.180-193314C=
XM_011521876.1:c.34+143798C=	XP_011520178.1:n.34+143798C=
XM_011521878.1:c.-327-193314C=	XP_011520180.1:n.-327-193314C=
XM_011521878.2:c.-327-193314C=	XP_011520180.1:n.-327-193314C=
XR_001751785.1:n.228+3750G=
XR_429539.2:n.7080+3750G=
XR_932322.1:n.7080+3750G=
XR_932323.1:n.6997-5120G=