Canonical Allele Identifier: CA2181537690

Gene: RORA

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.61116504G>T , CM000677.2:g.61116504G>T	GRCh38
NC_000015.9:g.61408703G>T , CM000677.1:g.61408703G>T	GRCh37
NC_000015.8:g.59195995G>T	NCBI36
NG_029246.1:g.117800C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335670.11:c.166+112549C>A MANE Select	ENSP00000335087.6:n.166+112549C>A
ENST00000335670.10:c.166+112549C>A	ENSP00000335087.6:n.166+112549C>A
ENST00000551975.5:c.81+112549C>A
ENST00000557822.5:n.191+112549C>A
ENST00000559145.1:n.173+112549C>A
ENST00000560300.1:n.182-75370C>A
ENST00000561093.1:n.179+112549C>A
NM_134261.2:c.166+112549C>A	NP_599023.1:n.166+112549C>A
XM_011521878.1:c.-328+112549C>A	XP_011520180.1:n.-328+112549C>A
XM_011521878.2:c.-328+112549C>A	XP_011520180.1:n.-328+112549C>A
XR_002957760.1:n.2765C>A
NM_134261.3:c.166+112549C>A MANE Select	NP_599023.1:n.166+112549C>A