Canonical Allele Identifier: CA479803645

Gene: NR4A1 NR4A1AS

Linked Data

• gnomAD v4: 12-52059412-T-C
• MyVariant Identifiers: chr12:g.52453196T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52059412T>C , CM000674.2:g.52059412T>C	GRCh38
NC_000012.11:g.52453196T>C , CM000674.1:g.52453196T>C	GRCh37
NC_000012.10:g.50739463T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000394825.6:c.*468T>C (NR4A1) MANE Select	ENSP00000378302.1:n.*468T>C
ENST00000243050.5:c.*468T>C (NR4A1)	ENSP00000243050.1:n.*468T>C
ENST00000360284.7:c.*468T>C (NR4A1)	ENSP00000353427.3:n.*468T>C
ENST00000394824.2:c.*468T>C (NR4A1)	ENSP00000378301.2:n.*468T>C
ENST00000394825.5:c.*468T>C (NR4A1)	ENSP00000378302.1:n.*468T>C
ENST00000545748.5:c.*468T>C (NR4A1)	ENSP00000440864.1:n.*468T>C
ENST00000550557.1:n.4746T>C (NR4A1)
NM_001202233.1:c.*468T>C (NR4A1)	NP_001189162.1:n.*468T>C
NM_001202234.1:c.*468T>C (NR4A1)	NP_001189163.1:n.*468T>C
NM_002135.4:c.*468T>C (NR4A1)	NP_002126.2:n.*468T>C
NM_173157.2:c.*468T>C (NR4A1)	NP_775180.1:n.*468T>C
XM_005268822.3:c.*468T>C (NR4A1)	XP_005268879.1:n.*468T>C
XM_005268824.2:c.*468T>C (NR4A1)	XP_005268881.1:n.*468T>C
XM_006719363.1:c.*468T>C (NR4A1)	XP_006719426.1:n.*468T>C
XM_006719364.2:c.*468T>C (NR4A1)	XP_006719427.1:n.*468T>C
XM_011538250.1:c.*468T>C (NR4A1)	XP_011536552.1:n.*468T>C
XM_005268824.3:c.*468T>C (NR4A1)	XP_005268881.1:n.*468T>C
XM_006719364.4:c.*468T>C (NR4A1)	XP_006719427.1:n.*468T>C
XM_017019247.1:c.*468T>C (NR4A1)	XP_016874736.1:n.*468T>C
NM_173157.3:c.*468T>C (NR4A1) MANE Select	NP_775180.1:n.*468T>C
NM_001202233.2:c.*468T>C (NR4A1)	NP_001189162.1:n.*468T>C
NM_001202234.2:c.*468T>C (NR4A1)	NP_001189163.1:n.*468T>C
NM_002135.5:c.*468T>C (NR4A1)	NP_002126.2:n.*468T>C
NR_170321.1:n.89A>G (NR4A1AS)