Canonical Allele Identifier: CA2181480923

Gene: RORA

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.60998337_60998338delinsTA , CM000677.2:g.60998337_60998338delinsTA	GRCh38
NC_000015.9:g.61290536_61290537delinsTA , CM000677.1:g.61290536_61290537delinsTA	GRCh37
NC_000015.8:g.59077828_59077829delinsTA	NCBI36
NG_029246.1:g.235966_235967delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335670.11:c.166+230715_166+230716delinsTA MANE Select	ENSP00000335087.6:n.166+230715_166+230716delinsTA
ENST00000335670.10:c.166+230715_166+230716delinsTA	ENSP00000335087.6:n.166+230715_166+230716delinsTA
ENST00000551975.5:c.81+230715_81+230716delinsTA
ENST00000557822.5:n.191+230715_191+230716delinsTA
ENST00000559145.1:n.173+230715_173+230716delinsTA
ENST00000561093.1:n.179+230715_179+230716delinsTA
NM_134261.2:c.166+230715_166+230716delinsTA	NP_599023.1:n.166+230715_166+230716delinsTA
XM_011521876.1:c.34+17460_34+17461delinsTA	XP_011520178.1:n.34+17460_34+17461delinsTA
XM_011521878.1:c.-328+230715_-328+230716delinsTA	XP_011520180.1:n.-328+230715_-328+230716delinsTA
XM_011521878.2:c.-328+230715_-328+230716delinsTA	XP_011520180.1:n.-328+230715_-328+230716delinsTA
NM_134261.3:c.166+230715_166+230716delinsTA MANE Select	NP_599023.1:n.166+230715_166+230716delinsTA