Canonical Allele Identifier: CA479804063

Gene: NR4A1

Linked Data

• MyVariant Identifiers: chr12:g.52453286A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52059502A>C , CM000674.2:g.52059502A>C	GRCh38
NC_000012.11:g.52453286A>C , CM000674.1:g.52453286A>C	GRCh37
NC_000012.10:g.50739553A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000394825.6:c.*558A>C MANE Select	ENSP00000378302.1:n.*558A>C
ENST00000243050.5:c.*558A>C	ENSP00000243050.1:n.*558A>C
ENST00000360284.7:c.*558A>C	ENSP00000353427.3:n.*558A>C
ENST00000394824.2:c.*558A>C	ENSP00000378301.2:n.*558A>C
ENST00000394825.5:c.*558A>C	ENSP00000378302.1:n.*558A>C
ENST00000550557.1:n.4836A>C
NM_001202233.1:c.*558A>C	NP_001189162.1:n.*558A>C
NM_001202234.1:c.*558A>C	NP_001189163.1:n.*558A>C
NM_002135.4:c.*558A>C	NP_002126.2:n.*558A>C
NM_173157.2:c.*558A>C	NP_775180.1:n.*558A>C
XM_005268822.3:c.*558A>C	XP_005268879.1:n.*558A>C
XM_005268824.2:c.*558A>C	XP_005268881.1:n.*558A>C
XM_006719363.1:c.*558A>C	XP_006719426.1:n.*558A>C
XM_006719364.2:c.*558A>C	XP_006719427.1:n.*558A>C
XM_011538250.1:c.*558A>C	XP_011536552.1:n.*558A>C
XM_005268824.3:c.*558A>C	XP_005268881.1:n.*558A>C
XM_006719364.4:c.*558A>C	XP_006719427.1:n.*558A>C
XM_017019247.1:c.*558A>C	XP_016874736.1:n.*558A>C
NM_173157.3:c.*558A>C MANE Select	NP_775180.1:n.*558A>C
NM_001202233.2:c.*558A>C	NP_001189162.1:n.*558A>C
NM_001202234.2:c.*558A>C	NP_001189163.1:n.*558A>C
NM_002135.5:c.*558A>C	NP_002126.2:n.*558A>C