Canonical Allele Identifier: CA2618875675

Gene: NR4A1

Linked Data

• gnomAD v4: 12-52054314-CCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52054322_52054323del , CM000674.2:g.52054322_52054323del	GRCh38
NC_000012.11:g.52448106_52448107del , CM000674.1:g.52448106_52448107del	GRCh37
NC_000012.10:g.50734373_50734374del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394825.6:c.-2-5_-2-4del MANE Select	ENSP00000378302.1:n.-2-5_-2-4del
ENST00000243050.5:c.-2-5_-2-4del	ENSP00000243050.1:n.-2-5_-2-4del
ENST00000360284.7:c.38-5_38-4del	ENSP00000353427.3:n.38-5_38-4del
ENST00000394824.2:c.-2-5_-2-4del	ENSP00000378301.2:n.-2-5_-2-4del
ENST00000394825.5:c.-2-5_-2-4del	ENSP00000378302.1:n.-2-5_-2-4del
ENST00000478250.1:n.186-5_186-4del
ENST00000545748.5:c.161-5_161-4del	ENSP00000440864.1:n.161-5_161-4del
ENST00000546842.5:c.38-5_38-4del	ENSP00000457070.1:n.38-5_38-4del
ENST00000547206.5:n.224-5_224-4del
ENST00000548232.1:c.-2-5_-2-4del	ENSP00000449587.1:n.-2-5_-2-4del
ENST00000548733.1:n.107-2172_107-2171del
ENST00000548977.5:c.38-5_38-4del	ENSP00000456633.1:n.38-5_38-4del
ENST00000549102.1:n.488-5_488-4del
ENST00000550082.5:c.38-5_38-4del	ENSP00000449539.1:n.38-5_38-4del
ENST00000550557.1:n.905_906del
ENST00000550763.1:c.-2-5_-2-4del	ENSP00000449858.1:n.-2-5_-2-4del
ENST00000562373.1:c.-104-5_-104-4del	ENSP00000455399.1:n.-104-5_-104-4del
NM_001202233.1:c.38-5_38-4del	NP_001189162.1:n.38-5_38-4del
NM_001202234.1:c.161-5_161-4del	NP_001189163.1:n.161-5_161-4del
NM_002135.4:c.-2-5_-2-4del	NP_002126.2:n.-2-5_-2-4del
NM_173157.2:c.-2-5_-2-4del	NP_775180.1:n.-2-5_-2-4del
XM_005268822.3:c.215-5_215-4del	XP_005268879.1:n.215-5_215-4del
XM_005268824.2:c.-2-5_-2-4del	XP_005268881.1:n.-2-5_-2-4del
XM_006719363.1:c.-2-5_-2-4del	XP_006719426.1:n.-2-5_-2-4del
XM_006719364.2:c.-2-5_-2-4del	XP_006719427.1:n.-2-5_-2-4del
XM_011538250.1:c.-2-5_-2-4del	XP_011536552.1:n.-2-5_-2-4del
XM_011538251.1:c.215-5_215-4del	XP_011536553.1:n.215-5_215-4del
XM_005268824.3:c.-2-5_-2-4del	XP_005268881.1:n.-2-5_-2-4del
XM_006719364.4:c.-2-5_-2-4del	XP_006719427.1:n.-2-5_-2-4del
XM_017019247.1:c.11-5_11-4del	XP_016874736.1:n.11-5_11-4del
NM_173157.3:c.-2-5_-2-4del MANE Select	NP_775180.1:n.-2-5_-2-4del
NM_001202233.2:c.38-5_38-4del	NP_001189162.1:n.38-5_38-4del
NM_001202234.2:c.161-5_161-4del	NP_001189163.1:n.161-5_161-4del
NM_002135.5:c.-2-5_-2-4del	NP_002126.2:n.-2-5_-2-4del