Canonical Allele Identifier: CA2580604762

Gene: RORA

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.61037589A>C , CM000677.2:g.61037589A>C	GRCh38
NC_000015.9:g.61329788A>C , CM000677.1:g.61329788A>C	GRCh37
NC_000015.8:g.59117080A>C	NCBI36
NG_029246.1:g.196715T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000335670.11:c.166+191464T>G MANE Select	ENSP00000335087.6:n.166+191464T>G
ENST00000335670.10:c.166+191464T>G	ENSP00000335087.6:n.166+191464T>G
ENST00000551975.5:c.81+191464T>G
ENST00000557822.5:n.191+191464T>G
ENST00000559145.1:n.173+191464T>G
ENST00000561093.1:n.179+191464T>G
NM_134261.2:c.166+191464T>G	NP_599023.1:n.166+191464T>G
XM_011521878.1:c.-328+191464T>G	XP_011520180.1:n.-328+191464T>G
XM_011521878.2:c.-328+191464T>G	XP_011520180.1:n.-328+191464T>G
XR_001751773.2:n.2536T>G
XR_001751776.2:n.1088+1448T>G
XR_001751777.2:n.967-2663T>G
XR_002957755.1:n.7561T>G
XR_002957756.1:n.4512T>G
XR_002957757.1:n.7561T>G
XR_002957758.1:n.7561T>G
XR_002957759.1:n.7561T>G
XR_002957760.1:n.11158T>G
XR_002957761.1:n.7561T>G
NM_134261.3:c.166+191464T>G MANE Select	NP_599023.1:n.166+191464T>G