Canonical Allele Identifier: CA618472580

Gene: RORA

Linked Data

• dbSNP Id: rs572384813
• gnomAD v2: 15-61290536-T-TA
• gnomAD v3: 15-60998337-T-TA
• gnomAD v4: 15-60998337-T-TA
• MyVariant Identifiers: chr15:g.61290536_61290537insA (hg19) ; chr15:g.60998337_60998338insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.60998344dup , CM000677.2:g.60998344dup	GRCh38
NC_000015.9:g.61290543dup , CM000677.1:g.61290543dup	GRCh37
NC_000015.8:g.59077835dup	NCBI36
NG_029246.1:g.235966dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335670.11:c.166+230715dup MANE Select	ENSP00000335087.6:n.166+230715dup
ENST00000335670.10:c.166+230715dup	ENSP00000335087.6:n.166+230715dup
ENST00000551975.5:c.81+230715dup
ENST00000557822.5:n.191+230715dup
ENST00000559145.1:n.173+230715dup
ENST00000561093.1:n.179+230715dup
NM_134261.2:c.166+230715dup	NP_599023.1:n.166+230715dup
XM_011521876.1:c.34+17460dup	XP_011520178.1:n.34+17460dup
XM_011521878.1:c.-328+230715dup	XP_011520180.1:n.-328+230715dup
XM_011521878.2:c.-328+230715dup	XP_011520180.1:n.-328+230715dup
NM_134261.3:c.166+230715dup MANE Select	NP_599023.1:n.166+230715dup