Canonical Allele Identifier: CA2618880269

Gene: NR4A1 NR4A1AS

Linked Data

• gnomAD v4: 12-52059301-C-CGCCTTCCTG

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52059303_52059311dup , CM000674.2:g.52059303_52059311dup	GRCh38
NC_000012.11:g.52453087_52453095dup , CM000674.1:g.52453087_52453095dup	GRCh37
NC_000012.10:g.50739354_50739362dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000394825.6:c.*359_*367dup (NR4A1) MANE Select	ENSP00000378302.1:n.*359_*367dup
ENST00000243050.5:c.*359_*367dup (NR4A1)	ENSP00000243050.1:n.*359_*367dup
ENST00000360284.7:c.*359_*367dup (NR4A1)	ENSP00000353427.3:n.*359_*367dup
ENST00000394824.2:c.*359_*367dup (NR4A1)	ENSP00000378301.2:n.*359_*367dup
ENST00000394825.5:c.*359_*367dup (NR4A1)	ENSP00000378302.1:n.*359_*367dup
ENST00000545748.5:c.*359_*367dup (NR4A1)	ENSP00000440864.1:n.*359_*367dup
ENST00000550557.1:n.4637_4645dup (NR4A1)
NM_001202233.1:c.*359_*367dup (NR4A1)	NP_001189162.1:n.*359_*367dup
NM_001202234.1:c.*359_*367dup (NR4A1)	NP_001189163.1:n.*359_*367dup
NM_002135.4:c.*359_*367dup (NR4A1)	NP_002126.2:n.*359_*367dup
NM_173157.2:c.*359_*367dup (NR4A1)	NP_775180.1:n.*359_*367dup
XM_005268822.3:c.*359_*367dup (NR4A1)	XP_005268879.1:n.*359_*367dup
XM_005268824.2:c.*359_*367dup (NR4A1)	XP_005268881.1:n.*359_*367dup
XM_006719363.1:c.*359_*367dup (NR4A1)	XP_006719426.1:n.*359_*367dup
XM_006719364.2:c.*359_*367dup (NR4A1)	XP_006719427.1:n.*359_*367dup
XM_011538250.1:c.*359_*367dup (NR4A1)	XP_011536552.1:n.*359_*367dup
XM_005268824.3:c.*359_*367dup (NR4A1)	XP_005268881.1:n.*359_*367dup
XM_006719364.4:c.*359_*367dup (NR4A1)	XP_006719427.1:n.*359_*367dup
XM_017019247.1:c.*359_*367dup (NR4A1)	XP_016874736.1:n.*359_*367dup
NM_173157.3:c.*359_*367dup (NR4A1) MANE Select	NP_775180.1:n.*359_*367dup
NM_001202233.2:c.*359_*367dup (NR4A1)	NP_001189162.1:n.*359_*367dup
NM_001202234.2:c.*359_*367dup (NR4A1)	NP_001189163.1:n.*359_*367dup
NM_002135.5:c.*359_*367dup (NR4A1)	NP_002126.2:n.*359_*367dup
NR_170321.1:n.191_199dup (NR4A1AS)