Canonical Allele Identifier: CA6574012
Gene: NR4A1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2701124

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52054373G>A , CM000674.2:g.52054373G>A GRCh38
NC_000012.11:g.52448157G>A , CM000674.1:g.52448157G>A GRCh37
NC_000012.10:g.50734424G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001202233.1:c.84G>A VV NP_001189162.1:p.Pro28=
NM_001202234.1:c.207G>A VV NP_001189163.1:p.Pro69=
NM_002135.4:c.45G>A VV NP_002126.2:p.Pro15=
NM_173157.2:c.45G>A VV NP_775180.1:p.Pro15=
XM_005268822.3:c.261G>A XP_005268879.1:p.Pro87=
XM_005268824.2:c.45G>A XP_005268881.1:p.Pro15=
XM_006719363.1:c.45G>A XP_006719426.1:p.Pro15=
XM_006719364.2:c.45G>A XP_006719427.1:p.Pro15=
XM_011538250.1:c.45G>A XP_011536552.1:p.Pro15=
XM_011538251.1:c.261G>A XP_011536553.1:p.Pro87=
XM_005268824.3:c.45G>A XP_005268881.1:p.Pro15=
XM_006719364.4:c.45G>A XP_006719427.1:p.Pro15=
XM_017019247.1:c.57G>A XP_016874736.1:p.Pro19=
NM_173157.3:c.45G>A VV MANE Preferred NP_775180.1:p.Pro15=
ENST00000243050.5:c.45G>A ENSP00000243050.1:p.Pro15=
ENST00000360284.7:c.84G>A ENSP00000353427.3:p.Pro28=
ENST00000394824.2:c.45G>A ENSP00000378301.2:p.Pro15=
ENST00000394825.5:c.45G>A ENSP00000378302.1:p.Pro15=
ENST00000478250.1:n.232G>A
ENST00000545748.5:c.207G>A ENSP00000440864.1:p.Pro69=
ENST00000546842.5:c.84G>A ENSP00000457070.1:p.Pro28=
ENST00000547206.5:n.270G>A
ENST00000548232.1:c.45G>A ENSP00000449587.1:p.Pro15=
ENST00000548733.1:n.107-2121G>A
ENST00000548977.5:c.84G>A ENSP00000456633.1:p.Pro28=
ENST00000549102.1:n.534G>A
ENST00000550082.5:c.84G>A ENSP00000449539.1:p.Pro28=
ENST00000550557.1:n.956G>A
ENST00000550763.1:c.45G>A ENSP00000449858.1:p.Pro15=
ENST00000562373.1:c.-58G>A ENSP00000455399.1:p.=