Canonical Allele Identifier: CA348680018

Gene: NR4A2

Linked Data

• MyVariant Identifiers: chr2:g.157182695A>T (hg19) ; chr2:g.156326183A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156326183A>T , CM000664.2:g.156326183A>T	GRCh38
NC_000002.11:g.157182695A>T , CM000664.1:g.157182695A>T	GRCh37
NC_000002.10:g.156890941A>T	NCBI36
NG_011821.1:g.11593T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1303T>A	ENSP00000514865.1:p.Phe435Ile
ENST00000700229.1:c.471T>A
ENST00000700230.1:c.1047T>A	ENSP00000514867.1:n.1047T>A
ENST00000700231.1:c.1432T>A	ENSP00000514868.1:p.Phe478Ile
ENST00000339562.9:c.1507T>A MANE Select	ENSP00000344479.4:p.Phe503Ile
ENST00000675870.1:c.*18T>A	ENSP00000502739.1:n.*18T>A
ENST00000339562.8:c.1507T>A	ENSP00000344479.4:p.Phe503Ile
ENST00000409108.6:c.1403T>A	ENSP00000386993.2:p.Leu468His
ENST00000409572.5:c.1507T>A	ENSP00000386747.1:p.Phe503Ile
ENST00000417764.5:c.*18T>A	ENSP00000415632.1:n.*18T>A
ENST00000417972.5:c.*18T>A	ENSP00000394671.1:n.*18T>A
ENST00000426264.5:c.1318T>A	ENSP00000389986.1:p.Phe440Ile
ENST00000429376.5:c.1214T>A	ENSP00000410952.1:p.Leu405His
NM_006186.3:c.1507T>A	NP_006177.1:p.Phe503Ile
XM_005246621.2:c.1540T>A	XP_005246678.1:p.Phe514Ile
XM_005246622.2:c.1318T>A	XP_005246679.1:p.Phe440Ile
XM_005246623.1:c.1318T>A	XP_005246680.1:p.Phe440Ile
XM_006712553.2:c.1465T>A	XP_006712616.1:p.Phe489Ile
XM_011511246.1:c.1436T>A	XP_011509548.1:p.Leu479His
XR_427087.2:n.3592T>A
NM_173173.2:c.1318T>A	NP_775265.1:p.Phe440Ile
XM_005246621.4:c.1540T>A	XP_005246678.1:p.Phe514Ile
XM_006712553.4:c.1465T>A	XP_006712616.1:p.Phe489Ile
XM_011511246.2:c.1436T>A	XP_011509548.1:p.Leu479His
XM_017004219.2:c.1507T>A	XP_016859708.1:p.Phe503Ile
XM_017004220.2:c.1432T>A	XP_016859709.1:p.Phe478Ile
XR_001738751.2:n.1754T>A
XR_001738752.2:n.1576T>A
XR_427087.4:n.1633T>A
NM_006186.4:c.1507T>A MANE Select	NP_006177.1:p.Phe503Ile
NM_173173.3:c.1318T>A	NP_775265.1:p.Phe440Ile