Canonical Allele Identifier: CA2181314473

Gene: RORA

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.60645203C= , CM000677.2:g.60645203C=	GRCh38
NC_000015.9:g.60937402C= , CM000677.1:g.60937402C=	GRCh37
NC_000015.8:g.58724694C=	NCBI36
NG_029246.1:g.589101G=

Transcript Alleles

HGVS	Amino-acid Change
NM_134261.3:c.196+33454G= MANE Select	NP_599023.1:n.196+33454G=
ENST00000335670.11:c.196+33454G= MANE Select	ENSP00000335087.6:n.196+33454G=
NM_134261.2:c.196+33454G=	NP_599023.1:n.196+33454G=
ENST00000335670.10:c.196+33454G=	ENSP00000335087.6:n.196+33454G=
ENST00000551975.5:c.193+31948G=
ENST00000557822.5:n.221+33454G=
ENST00000560004.5:n.151+33454G=
XM_005254584.3:c.58+33454G=	XP_005254641.1:n.58+33454G=
XM_005254584.5:c.58+33454G=	XP_005254641.1:n.58+33454G=
XM_011521875.1:c.139+33454G=	XP_011520177.1:n.139+33454G=
XM_011521875.2:c.139+33454G=	XP_011520177.1:n.139+33454G=
XM_011521876.1:c.64+33454G=	XP_011520178.1:n.64+33454G=
XM_011521878.1:c.-216+31948G=	XP_011520180.1:n.-216+31948G=
XM_011521878.2:c.-216+31948G=	XP_011520180.1:n.-216+31948G=
XR_001751783.2:n.4066+964C=
XR_932331.1:n.307+964C=