Canonical Allele Identifier: CA2181480896

Gene: RORA

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.60998286_60998288delinsCCT , CM000677.2:g.60998286_60998288delinsCCT	GRCh38
NC_000015.9:g.61290485_61290487delinsCCT , CM000677.1:g.61290485_61290487delinsCCT	GRCh37
NC_000015.8:g.59077777_59077779delinsCCT	NCBI36
NG_029246.1:g.236016_236018delinsAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335670.11:c.166+230765_166+230767delinsAGG MANE Select	ENSP00000335087.6:n.166+230765_166+230767delinsAGG
ENST00000335670.10:c.166+230765_166+230767delinsAGG	ENSP00000335087.6:n.166+230765_166+230767delinsAGG
ENST00000551975.5:c.81+230765_81+230767delinsAGG
ENST00000557822.5:n.191+230765_191+230767delinsAGG
ENST00000559145.1:n.173+230765_173+230767delinsAGG
ENST00000561093.1:n.179+230765_179+230767delinsAGG
NM_134261.2:c.166+230765_166+230767delinsAGG	NP_599023.1:n.166+230765_166+230767delinsAGG
XM_011521876.1:c.34+17510_34+17512delinsAGG	XP_011520178.1:n.34+17510_34+17512delinsAGG
XM_011521878.1:c.-328+230765_-328+230767delinsAGG	XP_011520180.1:n.-328+230765_-328+230767delinsAGG
XM_011521878.2:c.-328+230765_-328+230767delinsAGG	XP_011520180.1:n.-328+230765_-328+230767delinsAGG
NM_134261.3:c.166+230765_166+230767delinsAGG MANE Select	NP_599023.1:n.166+230765_166+230767delinsAGG