Canonical Allele Identifier: CA2036307158

Gene: NR4A1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52054305C= , CM000674.2:g.52054305C=	GRCh38
NC_000012.11:g.52448089C= , CM000674.1:g.52448089C=	GRCh37
NC_000012.10:g.50734356C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000394825.6:c.-2-22C= MANE Select	ENSP00000378302.1:n.-2-22C=
ENST00000243050.5:c.-2-22C=	ENSP00000243050.1:n.-2-22C=
ENST00000360284.7:c.38-22C=	ENSP00000353427.3:n.38-22C=
ENST00000394824.2:c.-2-22C=	ENSP00000378301.2:n.-2-22C=
ENST00000394825.5:c.-2-22C=	ENSP00000378302.1:n.-2-22C=
ENST00000478250.1:n.186-22C=
ENST00000545748.5:c.161-22C=	ENSP00000440864.1:n.161-22C=
ENST00000546842.5:c.38-22C=	ENSP00000457070.1:n.38-22C=
ENST00000547206.5:n.224-22C=
ENST00000548232.1:c.-2-22C=	ENSP00000449587.1:n.-2-22C=
ENST00000548733.1:n.107-2189C=
ENST00000548977.5:c.38-22C=	ENSP00000456633.1:n.38-22C=
ENST00000549102.1:n.488-22C=
ENST00000550082.5:c.38-22C=	ENSP00000449539.1:n.38-22C=
ENST00000550557.1:n.888C=
ENST00000550763.1:c.-2-22C=	ENSP00000449858.1:n.-2-22C=
ENST00000562373.1:c.-104-22C=	ENSP00000455399.1:n.-104-22C=
NM_001202233.1:c.38-22C=	NP_001189162.1:n.38-22C=
NM_001202234.1:c.161-22C=	NP_001189163.1:n.161-22C=
NM_002135.4:c.-2-22C=	NP_002126.2:n.-2-22C=
NM_173157.2:c.-2-22C=	NP_775180.1:n.-2-22C=
XM_005268822.3:c.215-22C=	XP_005268879.1:n.215-22C=
XM_005268824.2:c.-2-22C=	XP_005268881.1:n.-2-22C=
XM_006719363.1:c.-2-22C=	XP_006719426.1:n.-2-22C=
XM_006719364.2:c.-2-22C=	XP_006719427.1:n.-2-22C=
XM_011538250.1:c.-2-22C=	XP_011536552.1:n.-2-22C=
XM_011538251.1:c.215-22C=	XP_011536553.1:n.215-22C=
XM_005268824.3:c.-2-22C=	XP_005268881.1:n.-2-22C=
XM_006719364.4:c.-2-22C=	XP_006719427.1:n.-2-22C=
XM_017019247.1:c.11-22C=	XP_016874736.1:n.11-22C=
NM_173157.3:c.-2-22C= MANE Select	NP_775180.1:n.-2-22C=
NM_001202233.2:c.38-22C=	NP_001189162.1:n.38-22C=
NM_001202234.2:c.161-22C=	NP_001189163.1:n.161-22C=
NM_002135.5:c.-2-22C=	NP_002126.2:n.-2-22C=