Canonical Allele Identifier: CA2181480849

Gene: RORA

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.60998181_60998182delinsTG , CM000677.2:g.60998181_60998182delinsTG	GRCh38
NC_000015.9:g.61290380_61290381delinsTG , CM000677.1:g.61290380_61290381delinsTG	GRCh37
NC_000015.8:g.59077672_59077673delinsTG	NCBI36
NG_029246.1:g.236122_236123delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335670.11:c.166+230871_166+230872delinsCA MANE Select	ENSP00000335087.6:n.166+230871_166+230872delinsCA
ENST00000335670.10:c.166+230871_166+230872delinsCA	ENSP00000335087.6:n.166+230871_166+230872delinsCA
ENST00000551975.5:c.81+230871_81+230872delinsCA
ENST00000557822.5:n.191+230871_191+230872delinsCA
ENST00000559145.1:n.173+230871_173+230872delinsCA
ENST00000561093.1:n.179+230871_179+230872delinsCA
NM_134261.2:c.166+230871_166+230872delinsCA	NP_599023.1:n.166+230871_166+230872delinsCA
XM_011521876.1:c.34+17616_34+17617delinsCA	XP_011520178.1:n.34+17616_34+17617delinsCA
XM_011521878.1:c.-328+230871_-328+230872delinsCA	XP_011520180.1:n.-328+230871_-328+230872delinsCA
XM_011521878.2:c.-328+230871_-328+230872delinsCA	XP_011520180.1:n.-328+230871_-328+230872delinsCA
NM_134261.3:c.166+230871_166+230872delinsCA MANE Select	NP_599023.1:n.166+230871_166+230872delinsCA