Canonical Allele Identifier: CA272215370

Gene: RORA

Linked Data

• dbSNP Id: rs796596715

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.60998181_60998182delinsAC , CM000677.2:g.60998181_60998182delinsAC	GRCh38
NC_000015.9:g.61290380_61290381delinsAC , CM000677.1:g.61290380_61290381delinsAC	GRCh37
NC_000015.8:g.59077672_59077673delinsAC	NCBI36
NG_029246.1:g.236122_236123delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335670.11:c.166+230871_166+230872delinsGT MANE Select	ENSP00000335087.6:n.166+230871_166+230872delinsGT
ENST00000335670.10:c.166+230871_166+230872delinsGT	ENSP00000335087.6:n.166+230871_166+230872delinsGT
ENST00000551975.5:c.81+230871_81+230872delinsGT
ENST00000557822.5:n.191+230871_191+230872delinsGT
ENST00000559145.1:n.173+230871_173+230872delinsGT
ENST00000561093.1:n.179+230871_179+230872delinsGT
NM_134261.2:c.166+230871_166+230872delinsGT	NP_599023.1:n.166+230871_166+230872delinsGT
XM_011521876.1:c.34+17616_34+17617delinsGT	XP_011520178.1:n.34+17616_34+17617delinsGT
XM_011521878.1:c.-328+230871_-328+230872delinsGT	XP_011520180.1:n.-328+230871_-328+230872delinsGT
XM_011521878.2:c.-328+230871_-328+230872delinsGT	XP_011520180.1:n.-328+230871_-328+230872delinsGT
NM_134261.3:c.166+230871_166+230872delinsGT MANE Select	NP_599023.1:n.166+230871_166+230872delinsGT