Canonical Allele Identifier: CA2181480808

Gene: RORA

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.60998078_60998079delinsCA , CM000677.2:g.60998078_60998079delinsCA	GRCh38
NC_000015.9:g.61290277_61290278delinsCA , CM000677.1:g.61290277_61290278delinsCA	GRCh37
NC_000015.8:g.59077569_59077570delinsCA	NCBI36
NG_029246.1:g.236225_236226delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335670.11:c.166+230974_166+230975delinsTG MANE Select	ENSP00000335087.6:n.166+230974_166+230975delinsTG
ENST00000335670.10:c.166+230974_166+230975delinsTG	ENSP00000335087.6:n.166+230974_166+230975delinsTG
ENST00000551975.5:c.81+230974_81+230975delinsTG
ENST00000557822.5:n.191+230974_191+230975delinsTG
ENST00000559145.1:n.173+230974_173+230975delinsTG
ENST00000561093.1:n.179+230974_179+230975delinsTG
NM_134261.2:c.166+230974_166+230975delinsTG	NP_599023.1:n.166+230974_166+230975delinsTG
XM_011521876.1:c.34+17719_34+17720delinsTG	XP_011520178.1:n.34+17719_34+17720delinsTG
XM_011521878.1:c.-328+230974_-328+230975delinsTG	XP_011520180.1:n.-328+230974_-328+230975delinsTG
XM_011521878.2:c.-328+230974_-328+230975delinsTG	XP_011520180.1:n.-328+230974_-328+230975delinsTG
NM_134261.3:c.166+230974_166+230975delinsTG MANE Select	NP_599023.1:n.166+230974_166+230975delinsTG