Canonical Allele Identifier: CA2181480800

Gene: RORA

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.60998062G= , CM000677.2:g.60998062G=	GRCh38
NC_000015.9:g.61290261G= , CM000677.1:g.61290261G=	GRCh37
NC_000015.8:g.59077553G=	NCBI36
NG_029246.1:g.236242C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335670.11:c.166+230991C= MANE Select	ENSP00000335087.6:n.166+230991C=
ENST00000335670.10:c.166+230991C=	ENSP00000335087.6:n.166+230991C=
ENST00000551975.5:c.81+230991C=
ENST00000557822.5:n.191+230991C=
ENST00000559145.1:n.173+230991C=
ENST00000561093.1:n.179+230991C=
NM_134261.2:c.166+230991C=	NP_599023.1:n.166+230991C=
XM_011521876.1:c.34+17736C=	XP_011520178.1:n.34+17736C=
XM_011521878.1:c.-328+230991C=	XP_011520180.1:n.-328+230991C=
XM_011521878.2:c.-328+230991C=	XP_011520180.1:n.-328+230991C=
NM_134261.3:c.166+230991C= MANE Select	NP_599023.1:n.166+230991C=