Canonical Allele Identifier: CA15756071
Gene: NR4A1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2603751

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52059498T>C , CM000674.2:g.52059498T>C GRCh38
NC_000012.11:g.52453282T>C , CM000674.1:g.52453282T>C GRCh37
NC_000012.10:g.50739549T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001202233.1:c.*554T>C VV NP_001189162.1:p.=
NM_001202234.1:c.*554T>C VV NP_001189163.1:p.=
NM_002135.4:c.*554T>C VV NP_002126.2:p.=
NM_173157.2:c.*554T>C VV NP_775180.1:p.=
XM_005268822.3:c.*554T>C XP_005268879.1:p.=
XM_005268824.2:c.*554T>C XP_005268881.1:p.=
XM_006719363.1:c.*554T>C XP_006719426.1:p.=
XM_006719364.2:c.*554T>C XP_006719427.1:p.=
XM_011538250.1:c.*554T>C XP_011536552.1:p.=
XM_005268824.3:c.*554T>C XP_005268881.1:p.=
XM_006719364.4:c.*554T>C XP_006719427.1:p.=
XM_017019247.1:c.*554T>C XP_016874736.1:p.=
NM_173157.3:c.*554T>C VV MANE Preferred NP_775180.1:p.=
ENST00000243050.5:c.*554T>C ENSP00000243050.1:p.=
ENST00000360284.7:c.*554T>C ENSP00000353427.3:p.=
ENST00000394824.2:c.*554T>C ENSP00000378301.2:p.=
ENST00000394825.5:c.*554T>C ENSP00000378302.1:p.=
ENST00000545748.5:c.*554T>C ENSP00000440864.1:p.=
ENST00000550557.1:n.4832T>C