Canonical Allele Identifier: CA714594745

Gene: RORA

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.61139797C>A , CM000677.2:g.61139797C>A	GRCh38
NC_000015.9:g.61431996C>A , CM000677.1:g.61431996C>A	GRCh37
NC_000015.8:g.59219288C>A	NCBI36
NG_029246.1:g.94507G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335670.11:c.166+89256G>T MANE Select	ENSP00000335087.6:n.166+89256G>T
ENST00000335670.10:c.166+89256G>T	ENSP00000335087.6:n.166+89256G>T
ENST00000551975.5:c.81+89256G>T
ENST00000557822.5:n.191+89256G>T
ENST00000559145.1:n.173+89256G>T
ENST00000560300.1:n.181+89256G>T
ENST00000561093.1:n.179+89256G>T
NM_134261.2:c.166+89256G>T	NP_599023.1:n.166+89256G>T
XM_011521878.1:c.-328+89256G>T	XP_011520180.1:n.-328+89256G>T
XM_011521878.2:c.-328+89256G>T	XP_011520180.1:n.-328+89256G>T
NM_134261.3:c.166+89256G>T MANE Select	NP_599023.1:n.166+89256G>T