Canonical Allele Identifier: CA759316909

Gene: NR4A2

Linked Data

• dbSNP Id: rs1454453235
• MyVariant Identifiers: chr2:g.157186080_157186081insG (hg19) ; chr2:g.156329568_156329569insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156329571dup , CM000664.2:g.156329571dup	GRCh38
NC_000002.11:g.157186083dup , CM000664.1:g.157186083dup	GRCh37
NC_000002.10:g.156894329dup	NCBI36
NG_011821.1:g.8207dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421709.2:c.429dup	ENSP00000388120.2:p.Ala144ArgfsTer?
ENST00000700228.1:c.489dup	ENSP00000514865.1:p.Ala164ArgfsTer?
ENST00000700230.1:c.51dup	ENSP00000514867.1:p.Ala18ArgfsTer?
ENST00000700231.1:c.618dup	ENSP00000514868.1:p.Ala207ArgfsTer?
ENST00000339562.9:c.618dup MANE Select	ENSP00000344479.4:p.Ala207ArgfsTer?
ENST00000675870.1:c.429dup	ENSP00000502739.1:p.Ala144ArgfsTer?
ENST00000339562.8:c.618dup	ENSP00000344479.4:p.Ala207ArgfsTer?
ENST00000406048.2:c.208+345dup
ENST00000409108.6:c.618dup	ENSP00000386993.2:p.Ala207ArgfsTer?
ENST00000409572.5:c.618dup	ENSP00000386747.1:p.Ala207ArgfsTer?
ENST00000417764.5:c.429dup	ENSP00000415632.1:p.Ala144ArgfsTer?
ENST00000417972.5:c.429dup	ENSP00000394671.1:p.Ala144ArgfsTer?
ENST00000424077.1:c.618dup	ENSP00000406808.1:p.Ala207ArgfsTer?
ENST00000426264.5:c.429dup	ENSP00000389986.1:p.Ala144ArgfsTer?
ENST00000429376.5:c.429dup	ENSP00000410952.1:p.Ala144ArgfsTer?
NM_006186.3:c.618dup	NP_006177.1:p.Ala207ArgfsTer?
XM_005246621.2:c.651dup	XP_005246678.1:p.Ala218ArgfsTer?
XM_005246622.2:c.429dup	XP_005246679.1:p.Ala144ArgfsTer?
XM_005246623.1:c.429dup	XP_005246680.1:p.Ala144ArgfsTer?
XM_006712553.2:c.651dup	XP_006712616.1:p.Ala218ArgfsTer?
XM_011511246.1:c.651dup	XP_011509548.1:p.Ala218ArgfsTer?
XR_427087.2:n.2824dup
NM_173173.2:c.429dup	NP_775265.1:p.Ala144ArgfsTer?
XM_005246621.4:c.651dup	XP_005246678.1:p.Ala218ArgfsTer?
XM_006712553.4:c.651dup	XP_006712616.1:p.Ala218ArgfsTer?
XM_011511246.2:c.651dup	XP_011509548.1:p.Ala218ArgfsTer?
XM_017004219.2:c.618dup	XP_016859708.1:p.Ala207ArgfsTer?
XM_017004220.2:c.618dup	XP_016859709.1:p.Ala207ArgfsTer?
XR_001738751.2:n.986dup
XR_001738752.2:n.808dup
XR_427087.4:n.865dup
NM_006186.4:c.618dup MANE Select	NP_006177.1:p.Ala207ArgfsTer?
NM_173173.3:c.429dup	NP_775265.1:p.Ala144ArgfsTer?