Canonical Allele Identifier: CA2181553235

Gene: RORA

Linked Data

• dbSNP Id: rs2079370270

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.61148496_61148497del , CM000677.2:g.61148496_61148497del	GRCh38
NC_000015.9:g.61440695_61440696del , CM000677.1:g.61440695_61440696del	GRCh37
NC_000015.8:g.59227987_59227988del	NCBI36
NG_029246.1:g.85813_85814del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335670.11:c.166+80562_166+80563del MANE Select	ENSP00000335087.6:n.166+80562_166+80563del
ENST00000335670.10:c.166+80562_166+80563del	ENSP00000335087.6:n.166+80562_166+80563del
ENST00000551975.5:c.81+80562_81+80563del
ENST00000557822.5:n.191+80562_191+80563del
ENST00000559145.1:n.173+80562_173+80563del
ENST00000560300.1:n.181+80562_181+80563del
ENST00000561093.1:n.179+80562_179+80563del
NM_134261.2:c.166+80562_166+80563del	NP_599023.1:n.166+80562_166+80563del
XM_011521878.1:c.-328+80562_-328+80563del	XP_011520180.1:n.-328+80562_-328+80563del
XM_011521878.2:c.-328+80562_-328+80563del	XP_011520180.1:n.-328+80562_-328+80563del
NM_134261.3:c.166+80562_166+80563del MANE Select	NP_599023.1:n.166+80562_166+80563del