Canonical Allele Identifier: CA2181480904

Gene: RORA

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.60998304_60998305delinsCA , CM000677.2:g.60998304_60998305delinsCA	GRCh38
NC_000015.9:g.61290503_61290504delinsCA , CM000677.1:g.61290503_61290504delinsCA	GRCh37
NC_000015.8:g.59077795_59077796delinsCA	NCBI36
NG_029246.1:g.235999_236000delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335670.11:c.166+230748_166+230749delinsTG MANE Select	ENSP00000335087.6:n.166+230748_166+230749delinsTG
ENST00000335670.10:c.166+230748_166+230749delinsTG	ENSP00000335087.6:n.166+230748_166+230749delinsTG
ENST00000551975.5:c.81+230748_81+230749delinsTG
ENST00000557822.5:n.191+230748_191+230749delinsTG
ENST00000559145.1:n.173+230748_173+230749delinsTG
ENST00000561093.1:n.179+230748_179+230749delinsTG
NM_134261.2:c.166+230748_166+230749delinsTG	NP_599023.1:n.166+230748_166+230749delinsTG
XM_011521876.1:c.34+17493_34+17494delinsTG	XP_011520178.1:n.34+17493_34+17494delinsTG
XM_011521878.1:c.-328+230748_-328+230749delinsTG	XP_011520180.1:n.-328+230748_-328+230749delinsTG
XM_011521878.2:c.-328+230748_-328+230749delinsTG	XP_011520180.1:n.-328+230748_-328+230749delinsTG
NM_134261.3:c.166+230748_166+230749delinsTG MANE Select	NP_599023.1:n.166+230748_166+230749delinsTG