Canonical Allele Identifier: CA2181553155

Gene: RORA

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.61148290_61148291delinsTC , CM000677.2:g.61148290_61148291delinsTC	GRCh38
NC_000015.9:g.61440489_61440490delinsTC , CM000677.1:g.61440489_61440490delinsTC	GRCh37
NC_000015.8:g.59227781_59227782delinsTC	NCBI36
NG_029246.1:g.86013_86014delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335670.11:c.166+80762_166+80763delinsGA MANE Select	ENSP00000335087.6:n.166+80762_166+80763delinsGA
ENST00000335670.10:c.166+80762_166+80763delinsGA	ENSP00000335087.6:n.166+80762_166+80763delinsGA
ENST00000551975.5:c.81+80762_81+80763delinsGA
ENST00000557822.5:n.191+80762_191+80763delinsGA
ENST00000559145.1:n.173+80762_173+80763delinsGA
ENST00000560300.1:n.181+80762_181+80763delinsGA
ENST00000561093.1:n.179+80762_179+80763delinsGA
NM_134261.2:c.166+80762_166+80763delinsGA	NP_599023.1:n.166+80762_166+80763delinsGA
XM_011521878.1:c.-328+80762_-328+80763delinsGA	XP_011520180.1:n.-328+80762_-328+80763delinsGA
XM_011521878.2:c.-328+80762_-328+80763delinsGA	XP_011520180.1:n.-328+80762_-328+80763delinsGA
NM_134261.3:c.166+80762_166+80763delinsGA MANE Select	NP_599023.1:n.166+80762_166+80763delinsGA