Canonical Allele Identifier: CA970530509

Gene: RORA

Linked Data

• gnomAD v3: 15-61148308-T-TCACCTGAATGCCAGCATCCAACTGACACAAAGCTGTGGAAGAGGAGGTATGGTCCTTAACACAGCTTTGTG
• gnomAD v4: 15-61148308-T-TCACCTGAATGCCAGCATCCAACTGACACAAAGCTGTGGAAGAGGAGGTATGGTCCTTAACACAGCTTTGTG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.61148308_61148309insCACCTGAATGCCAGCATCCAACTGACACAAAGCTGTGGAAGAGGAGGTATGGTCCTTAACACAGCTTTGTG , CM000677.2:g.61148308_61148309insCACCTGAATGCCAGCATCCAACTGACACAAAGCTGTGGAAGAGGAGGTATGGTCCTTAACACAGCTTTGTG	GRCh38
NC_000015.9:g.61440507_61440508insCACCTGAATGCCAGCATCCAACTGACACAAAGCTGTGGAAGAGGAGGTATGGTCCTTAACACAGCTTTGTG , CM000677.1:g.61440507_61440508insCACCTGAATGCCAGCATCCAACTGACACAAAGCTGTGGAAGAGGAGGTATGGTCCTTAACACAGCTTTGTG	GRCh37
NC_000015.8:g.59227799_59227800insCACCTGAATGCCAGCATCCAACTGACACAAAGCTGTGGAAGAGGAGGTATGGTCCTTAACACAGCTTTGTG	NCBI36
NG_029246.1:g.85995_85996insCACAAAGCTGTGTTAAGGACCATACCTCCTCTTCCACAGCTTTGTGTCAGTTGGATGCTGGCATTCAGGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335670.11:c.166+80744_166+80745insCACAAAGCTGTGTTAAGGACCATACCTCCTCTTCCACAGCTTTGTGTCAGTTGGATGCTGGCATTCAGGTG MANE Select	ENSP00000335087.6:n.166+80744_166+80745insCACAAAGCTGTGTTAAGGA...
ENST00000335670.10:c.166+80744_166+80745insCACAAAGCTGTGTTAAGGACCATACCTCCTCTTCCACAGCTTTGTGTCAGTTGGATGCTGGCATTCAGGTG	ENSP00000335087.6:n.166+80744_166+80745insCACAAAGCTGTGTTAAGGA...
ENST00000551975.5:c.81+80744_81+80745insCACAAAGCTGTGTTAAGGACCATACCTCCTCTTCCACAGCTTTGTGTCAGTTGGATGCTGGCATTCAGGTG
ENST00000557822.5:n.191+80744_191+80745insCACAAAGCTGTGTTAAGGACCATACCTCCTCTTCCACAGCTTTGTGTCAGTTGGATGCTGGCATTCAGGTG
ENST00000559145.1:n.173+80744_173+80745insCACAAAGCTGTGTTAAGGACCATACCTCCTCTTCCACAGCTTTGTGTCAGTTGGATGCTGGCATTCAGGTG
ENST00000560300.1:n.181+80744_181+80745insCACAAAGCTGTGTTAAGGACCATACCTCCTCTTCCACAGCTTTGTGTCAGTTGGATGCTGGCATTCAGGTG
ENST00000561093.1:n.179+80744_179+80745insCACAAAGCTGTGTTAAGGACCATACCTCCTCTTCCACAGCTTTGTGTCAGTTGGATGCTGGCATTCAGGTG
NM_134261.2:c.166+80744_166+80745insCACAAAGCTGTGTTAAGGACCATACCTCCTCTTCCACAGCTTTGTGTCAGTTGGATGCTGGCATTCAGGTG	NP_599023.1:n.166+80744_166+80745insCACAAAGCTGTGTTAAGGACCATAC...
XM_011521878.1:c.-328+80744_-328+80745insCACAAAGCTGTGTTAAGGACCATACCTCCTCTTCCACAGCTTTGTGTCAGTTGGATGCTGGCATTCAGGTG	XP_011520180.1:n.-328+80744_-328+80745insCACAAAGCTGTGTTAAGGAC...
XM_011521878.2:c.-328+80744_-328+80745insCACAAAGCTGTGTTAAGGACCATACCTCCTCTTCCACAGCTTTGTGTCAGTTGGATGCTGGCATTCAGGTG	XP_011520180.1:n.-328+80744_-328+80745insCACAAAGCTGTGTTAAGGAC...
NM_134261.3:c.166+80744_166+80745insCACAAAGCTGTGTTAAGGACCATACCTCCTCTTCCACAGCTTTGTGTCAGTTGGATGCTGGCATTCAGGTG MANE Select	NP_599023.1:n.166+80744_166+80745insCACAAAGCTGTGTTAAGGACCATAC...