Canonical Allele Identifier: CA714566693

Gene: RORA

Linked Data

• dbSNP Id: rs1396129877
• MyVariant Identifiers: chr15:g.61290530_61290531insT (hg19) ; chr15:g.60998331_60998332insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.60998337dup , CM000677.2:g.60998337dup	GRCh38
NC_000015.9:g.61290536dup , CM000677.1:g.61290536dup	GRCh37
NC_000015.8:g.59077828dup	NCBI36
NG_029246.1:g.235972dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335670.11:c.166+230721dup MANE Select	ENSP00000335087.6:n.166+230721dup
ENST00000335670.10:c.166+230721dup	ENSP00000335087.6:n.166+230721dup
ENST00000551975.5:c.81+230721dup
ENST00000557822.5:n.191+230721dup
ENST00000559145.1:n.173+230721dup
ENST00000561093.1:n.179+230721dup
NM_134261.2:c.166+230721dup	NP_599023.1:n.166+230721dup
XM_011521876.1:c.34+17466dup	XP_011520178.1:n.34+17466dup
XM_011521878.1:c.-328+230721dup	XP_011520180.1:n.-328+230721dup
XM_011521878.2:c.-328+230721dup	XP_011520180.1:n.-328+230721dup
NM_134261.3:c.166+230721dup MANE Select	NP_599023.1:n.166+230721dup