Canonical Allele Identifier: CA2036316808
Gene: NR4A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52059501G= , CM000674.2:g.52059501G= GRCh38
NC_000012.11:g.52453285G= , CM000674.1:g.52453285G= GRCh37
NC_000012.10:g.50739552G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000394825.6:c.*557G= MANE Select ENSP00000378302.1:n.*557G=
ENST00000243050.5:c.*557G= ENSP00000243050.1:n.*557G=
ENST00000360284.7:c.*557G= ENSP00000353427.3:n.*557G=
ENST00000394824.2:c.*557G= ENSP00000378301.2:n.*557G=
ENST00000394825.5:c.*557G= ENSP00000378302.1:n.*557G=
ENST00000545748.5:c.*557G= ENSP00000440864.1:n.*557G=
ENST00000550557.1:n.4835G=
NM_001202233.1:c.*557G= NP_001189162.1:n.*557G=
NM_001202234.1:c.*557G= NP_001189163.1:n.*557G=
NM_002135.4:c.*557G= NP_002126.2:n.*557G=
NM_173157.2:c.*557G= NP_775180.1:n.*557G=
XM_005268822.3:c.*557G= XP_005268879.1:n.*557G=
XM_005268824.2:c.*557G= XP_005268881.1:n.*557G=
XM_006719363.1:c.*557G= XP_006719426.1:n.*557G=
XM_006719364.2:c.*557G= XP_006719427.1:n.*557G=
XM_011538250.1:c.*557G= XP_011536552.1:n.*557G=
XM_005268824.3:c.*557G= XP_005268881.1:n.*557G=
XM_006719364.4:c.*557G= XP_006719427.1:n.*557G=
XM_017019247.1:c.*557G= XP_016874736.1:n.*557G=
NM_173157.3:c.*557G= MANE Select NP_775180.1:n.*557G=
NM_001202233.2:c.*557G= NP_001189162.1:n.*557G=
NM_001202234.2:c.*557G= NP_001189163.1:n.*557G=
NM_002135.5:c.*557G= NP_002126.2:n.*557G=