Canonical Allele Identifier: CA2181480895

Gene: RORA

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.60998284C= , CM000677.2:g.60998284C=	GRCh38
NC_000015.9:g.61290483C= , CM000677.1:g.61290483C=	GRCh37
NC_000015.8:g.59077775C=	NCBI36
NG_029246.1:g.236020G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335670.11:c.166+230769G= MANE Select	ENSP00000335087.6:n.166+230769G=
ENST00000335670.10:c.166+230769G=	ENSP00000335087.6:n.166+230769G=
ENST00000551975.5:c.81+230769G=
ENST00000557822.5:n.191+230769G=
ENST00000559145.1:n.173+230769G=
ENST00000561093.1:n.179+230769G=
NM_134261.2:c.166+230769G=	NP_599023.1:n.166+230769G=
XM_011521876.1:c.34+17514G=	XP_011520178.1:n.34+17514G=
XM_011521878.1:c.-328+230769G=	XP_011520180.1:n.-328+230769G=
XM_011521878.2:c.-328+230769G=	XP_011520180.1:n.-328+230769G=
NM_134261.3:c.166+230769G= MANE Select	NP_599023.1:n.166+230769G=