Canonical Allele Identifier: CA2181374253

Gene: RORA

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.60777699C= , CM000677.2:g.60777699C=	GRCh38
NC_000015.9:g.61069898C= , CM000677.1:g.61069898C=	GRCh37
NC_000015.8:g.58857190C=	NCBI36
NG_029246.1:g.456605G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335670.11:c.167-99013G= MANE Select	ENSP00000335087.6:n.167-99013G=
ENST00000335670.10:c.167-99013G=	ENSP00000335087.6:n.167-99013G=
ENST00000551975.5:c.82-99013G=
ENST00000557822.5:n.192-99013G=
ENST00000559145.1:n.174-99013G=
ENST00000561093.1:n.180-99013G=
NM_134261.2:c.167-99013G=	NP_599023.1:n.167-99013G=
XM_005254584.3:c.28+63371G=	XP_005254641.1:n.28+63371G=
XM_011521876.1:c.35-99013G=	XP_011520178.1:n.35-99013G=
XM_011521878.1:c.-327-99013G=	XP_011520180.1:n.-327-99013G=
XM_005254584.5:c.28+63371G=	XP_005254641.1:n.28+63371G=
XM_011521878.2:c.-327-99013G=	XP_011520180.1:n.-327-99013G=
NM_134261.3:c.167-99013G= MANE Select	NP_599023.1:n.167-99013G=