Canonical Allele Identifier: CA429586163

Gene: NR4A2

Linked Data

• MyVariant Identifiers: chr2:g.157182268A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325756A>T , CM000664.2:g.156325756A>T	GRCh38
NC_000002.11:g.157182268A>T , CM000664.1:g.157182268A>T	GRCh37
NC_000002.10:g.156890514A>T	NCBI36
NG_011821.1:g.12020T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1581T>A	ENSP00000514865.1:p.Thr527=
ENST00000700229.1:c.749T>A
ENST00000700230.1:c.1325T>A	ENSP00000514867.1:n.1325T>A
ENST00000700231.1:c.1710T>A	ENSP00000514868.1:p.Thr570=
ENST00000339562.9:c.1785T>A MANE Select	ENSP00000344479.4:p.Thr595=
ENST00000675870.1:c.*296T>A	ENSP00000502739.1:n.*296T>A
ENST00000339562.8:c.1785T>A	ENSP00000344479.4:p.Thr595=
ENST00000409108.6:c.*19T>A	ENSP00000386993.2:n.*19T>A
ENST00000409572.5:c.1785T>A	ENSP00000386747.1:p.Thr595=
ENST00000417764.5:c.*296T>A	ENSP00000415632.1:n.*296T>A
ENST00000417972.5:c.*296T>A	ENSP00000394671.1:n.*296T>A
ENST00000426264.5:c.1596T>A	ENSP00000389986.1:p.Thr532=
ENST00000429376.5:c.*19T>A	ENSP00000410952.1:n.*19T>A
NM_006186.3:c.1785T>A	NP_006177.1:p.Thr595=
XM_005246621.2:c.1818T>A	XP_005246678.1:p.Thr606=
XM_005246622.2:c.1596T>A	XP_005246679.1:p.Thr532=
XM_005246623.1:c.1596T>A	XP_005246680.1:p.Thr532=
XM_006712553.2:c.1743T>A	XP_006712616.1:p.Thr581=
XM_011511246.1:c.*19T>A	XP_011509548.1:n.*19T>A
NM_173173.2:c.1596T>A	NP_775265.1:p.Thr532=
XM_005246621.4:c.1818T>A	XP_005246678.1:p.Thr606=
XM_006712553.4:c.1743T>A	XP_006712616.1:p.Thr581=
XM_011511246.2:c.*19T>A	XP_011509548.1:n.*19T>A
XM_017004219.2:c.1785T>A	XP_016859708.1:p.Thr595=
XM_017004220.2:c.1710T>A	XP_016859709.1:p.Thr570=
XR_001738751.2:n.2032T>A
XR_001738752.2:n.1854T>A
XR_427087.4:n.1911T>A
NM_006186.4:c.1785T>A MANE Select	NP_006177.1:p.Thr595=
NM_173173.3:c.1596T>A	NP_775265.1:p.Thr532=