Canonical Allele Identifier: CA479803628

Gene: NR4A1 NR4A1AS

Linked Data

• MyVariant Identifiers: chr12:g.52453193C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52059409C>T , CM000674.2:g.52059409C>T	GRCh38
NC_000012.11:g.52453193C>T , CM000674.1:g.52453193C>T	GRCh37
NC_000012.10:g.50739460C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000394825.6:c.*465C>T (NR4A1) MANE Select	ENSP00000378302.1:n.*465C>T
ENST00000243050.5:c.*465C>T (NR4A1)	ENSP00000243050.1:n.*465C>T
ENST00000360284.7:c.*465C>T (NR4A1)	ENSP00000353427.3:n.*465C>T
ENST00000394824.2:c.*465C>T (NR4A1)	ENSP00000378301.2:n.*465C>T
ENST00000394825.5:c.*465C>T (NR4A1)	ENSP00000378302.1:n.*465C>T
ENST00000545748.5:c.*465C>T (NR4A1)	ENSP00000440864.1:n.*465C>T
ENST00000550557.1:n.4743C>T (NR4A1)
NM_001202233.1:c.*465C>T (NR4A1)	NP_001189162.1:n.*465C>T
NM_001202234.1:c.*465C>T (NR4A1)	NP_001189163.1:n.*465C>T
NM_002135.4:c.*465C>T (NR4A1)	NP_002126.2:n.*465C>T
NM_173157.2:c.*465C>T (NR4A1)	NP_775180.1:n.*465C>T
XM_005268822.3:c.*465C>T (NR4A1)	XP_005268879.1:n.*465C>T
XM_005268824.2:c.*465C>T (NR4A1)	XP_005268881.1:n.*465C>T
XM_006719363.1:c.*465C>T (NR4A1)	XP_006719426.1:n.*465C>T
XM_006719364.2:c.*465C>T (NR4A1)	XP_006719427.1:n.*465C>T
XM_011538250.1:c.*465C>T (NR4A1)	XP_011536552.1:n.*465C>T
XM_005268824.3:c.*465C>T (NR4A1)	XP_005268881.1:n.*465C>T
XM_006719364.4:c.*465C>T (NR4A1)	XP_006719427.1:n.*465C>T
XM_017019247.1:c.*465C>T (NR4A1)	XP_016874736.1:n.*465C>T
NM_173157.3:c.*465C>T (NR4A1) MANE Select	NP_775180.1:n.*465C>T
NM_001202233.2:c.*465C>T (NR4A1)	NP_001189162.1:n.*465C>T
NM_001202234.2:c.*465C>T (NR4A1)	NP_001189163.1:n.*465C>T
NM_002135.5:c.*465C>T (NR4A1)	NP_002126.2:n.*465C>T
NR_170321.1:n.92G>A (NR4A1AS)