Canonical Allele Identifier: CA714509294

Gene: RORA

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.60666852C>G , CM000677.2:g.60666852C>G	GRCh38
NC_000015.9:g.60959051C>G , CM000677.1:g.60959051C>G	GRCh37
NC_000015.8:g.58746343C>G	NCBI36
NG_029246.1:g.567452G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335670.11:c.196+11805G>C MANE Select	ENSP00000335087.6:n.196+11805G>C
ENST00000335670.10:c.196+11805G>C	ENSP00000335087.6:n.196+11805G>C
ENST00000551975.5:c.193+10299G>C
ENST00000557822.5:n.221+11805G>C
ENST00000559145.1:n.285+10299G>C
ENST00000560004.5:n.151+11805G>C
NM_134261.2:c.196+11805G>C	NP_599023.1:n.196+11805G>C
XM_005254584.3:c.58+11805G>C	XP_005254641.1:n.58+11805G>C
XM_011521875.1:c.139+11805G>C	XP_011520177.1:n.139+11805G>C
XM_011521876.1:c.64+11805G>C	XP_011520178.1:n.64+11805G>C
XM_011521878.1:c.-216+10299G>C	XP_011520180.1:n.-216+10299G>C
XM_005254584.5:c.58+11805G>C	XP_005254641.1:n.58+11805G>C
XM_011521875.2:c.139+11805G>C	XP_011520177.1:n.139+11805G>C
XM_011521878.2:c.-216+10299G>C	XP_011520180.1:n.-216+10299G>C
NM_134261.3:c.196+11805G>C MANE Select	NP_599023.1:n.196+11805G>C