Canonical Allele Identifier: CA480063545

Gene: NR4A1

Linked Data

• MyVariant Identifiers: chr12:g.52448172C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52054388C>T , CM000674.2:g.52054388C>T	GRCh38
NC_000012.11:g.52448172C>T , CM000674.1:g.52448172C>T	GRCh37
NC_000012.10:g.50734439C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394825.6:c.60C>T MANE Select	ENSP00000378302.1:p.His20=
ENST00000243050.5:c.60C>T	ENSP00000243050.1:p.His20=
ENST00000360284.7:c.99C>T	ENSP00000353427.3:p.His33=
ENST00000394824.2:c.60C>T	ENSP00000378301.2:p.His20=
ENST00000394825.5:c.60C>T	ENSP00000378302.1:p.His20=
ENST00000478250.1:n.247C>T
ENST00000545748.5:c.222C>T	ENSP00000440864.1:p.His74=
ENST00000546842.5:c.99C>T	ENSP00000457070.1:p.His33=
ENST00000547206.5:n.285C>T
ENST00000548232.1:c.60C>T	ENSP00000449587.1:p.His20=
ENST00000548733.1:n.107-2106C>T
ENST00000548977.5:c.99C>T	ENSP00000456633.1:p.His33=
ENST00000549102.1:n.549C>T
ENST00000550082.5:c.99C>T	ENSP00000449539.1:p.His33=
ENST00000550557.1:n.971C>T
ENST00000550763.1:c.60C>T	ENSP00000449858.1:p.His20=
ENST00000562373.1:c.-43C>T	ENSP00000455399.1:n.-43C>T
NM_001202233.1:c.99C>T	NP_001189162.1:p.His33=
NM_001202234.1:c.222C>T	NP_001189163.1:p.His74=
NM_002135.4:c.60C>T	NP_002126.2:p.His20=
NM_173157.2:c.60C>T	NP_775180.1:p.His20=
XM_005268822.3:c.276C>T	XP_005268879.1:p.His92=
XM_005268824.2:c.60C>T	XP_005268881.1:p.His20=
XM_006719363.1:c.60C>T	XP_006719426.1:p.His20=
XM_006719364.2:c.60C>T	XP_006719427.1:p.His20=
XM_011538250.1:c.60C>T	XP_011536552.1:p.His20=
XM_011538251.1:c.276C>T	XP_011536553.1:p.His92=
XM_005268824.3:c.60C>T	XP_005268881.1:p.His20=
XM_006719364.4:c.60C>T	XP_006719427.1:p.His20=
XM_017019247.1:c.72C>T	XP_016874736.1:p.His24=
NM_173157.3:c.60C>T MANE Select	NP_775180.1:p.His20=
NM_001202233.2:c.99C>T	NP_001189162.1:p.His33=
NM_001202234.2:c.222C>T	NP_001189163.1:p.His74=
NM_002135.5:c.60C>T	NP_002126.2:p.His20=