Canonical Allele Identifier: CA618472572

Gene: RORA

Linked Data

• dbSNP Id: rs1195508587
• gnomAD v2: 15-61290485-CCT-C
• gnomAD v3: 15-60998286-CCT-C
• gnomAD v4: 15-60998286-CCT-C
• MyVariant Identifiers: chr15:g.61290486_61290487del (hg19) ; chr15:g.60998287_60998288del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.60998287_60998288del , CM000677.2:g.60998287_60998288del	GRCh38
NC_000015.9:g.61290486_61290487del , CM000677.1:g.61290486_61290487del	GRCh37
NC_000015.8:g.59077778_59077779del	NCBI36
NG_029246.1:g.236016_236017del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335670.11:c.166+230765_166+230766del MANE Select	ENSP00000335087.6:n.166+230765_166+230766del
ENST00000335670.10:c.166+230765_166+230766del	ENSP00000335087.6:n.166+230765_166+230766del
ENST00000551975.5:c.81+230765_81+230766del
ENST00000557822.5:n.191+230765_191+230766del
ENST00000559145.1:n.173+230765_173+230766del
ENST00000561093.1:n.179+230765_179+230766del
NM_134261.2:c.166+230765_166+230766del	NP_599023.1:n.166+230765_166+230766del
XM_011521876.1:c.34+17510_34+17511del	XP_011520178.1:n.34+17510_34+17511del
XM_011521878.1:c.-328+230765_-328+230766del	XP_011520180.1:n.-328+230765_-328+230766del
XM_011521878.2:c.-328+230765_-328+230766del	XP_011520180.1:n.-328+230765_-328+230766del
NM_134261.3:c.166+230765_166+230766del MANE Select	NP_599023.1:n.166+230765_166+230766del