Canonical Allele Identifier: CA970507596

Gene: RORA

Linked Data

• gnomAD v3: 15-60998188-G-GTTTTTTT
• gnomAD v4: 15-60998188-G-GTTTTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.60998188_60998189insTTTTTTT , CM000677.2:g.60998188_60998189insTTTTTTT	GRCh38
NC_000015.9:g.61290387_61290388insTTTTTTT , CM000677.1:g.61290387_61290388insTTTTTTT	GRCh37
NC_000015.8:g.59077679_59077680insTTTTTTT	NCBI36
NG_029246.1:g.236115_236116insAAAAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335670.11:c.166+230864_166+230865insAAAAAAA MANE Select	ENSP00000335087.6:n.166+230864_166+230865insAAAAAAA
ENST00000335670.10:c.166+230864_166+230865insAAAAAAA	ENSP00000335087.6:n.166+230864_166+230865insAAAAAAA
ENST00000551975.5:c.81+230864_81+230865insAAAAAAA
ENST00000557822.5:n.191+230864_191+230865insAAAAAAA
ENST00000559145.1:n.173+230864_173+230865insAAAAAAA
ENST00000561093.1:n.179+230864_179+230865insAAAAAAA
NM_134261.2:c.166+230864_166+230865insAAAAAAA	NP_599023.1:n.166+230864_166+230865insAAAAAAA
XM_011521876.1:c.34+17609_34+17610insAAAAAAA	XP_011520178.1:n.34+17609_34+17610insAAAAAAA
XM_011521878.1:c.-328+230864_-328+230865insAAAAAAA	XP_011520180.1:n.-328+230864_-328+230865insAAAAAAA
XM_011521878.2:c.-328+230864_-328+230865insAAAAAAA	XP_011520180.1:n.-328+230864_-328+230865insAAAAAAA
NM_134261.3:c.166+230864_166+230865insAAAAAAA MANE Select	NP_599023.1:n.166+230864_166+230865insAAAAAAA