Canonical Allele Identifier: CA429586158

Gene: NR4A2

Linked Data

• MyVariant Identifiers: chr2:g.157182262A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325750A>G , CM000664.2:g.156325750A>G	GRCh38
NC_000002.11:g.157182262A>G , CM000664.1:g.157182262A>G	GRCh37
NC_000002.10:g.156890508A>G	NCBI36
NG_011821.1:g.12026T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1587T>C	ENSP00000514865.1:p.Pro529=
ENST00000700229.1:c.755T>C
ENST00000700230.1:c.1331T>C	ENSP00000514867.1:n.1331T>C
ENST00000700231.1:c.1716T>C	ENSP00000514868.1:p.Pro572=
ENST00000339562.9:c.1791T>C MANE Select	ENSP00000344479.4:p.Pro597=
ENST00000675870.1:c.*302T>C	ENSP00000502739.1:n.*302T>C
ENST00000339562.8:c.1791T>C	ENSP00000344479.4:p.Pro597=
ENST00000409108.6:c.*25T>C	ENSP00000386993.2:n.*25T>C
ENST00000409572.5:c.1791T>C	ENSP00000386747.1:p.Pro597=
ENST00000417764.5:c.*302T>C	ENSP00000415632.1:n.*302T>C
ENST00000417972.5:c.*302T>C	ENSP00000394671.1:n.*302T>C
ENST00000426264.5:c.1602T>C	ENSP00000389986.1:p.Pro534=
ENST00000429376.5:c.*25T>C	ENSP00000410952.1:n.*25T>C
NM_006186.3:c.1791T>C	NP_006177.1:p.Pro597=
XM_005246621.2:c.1824T>C	XP_005246678.1:p.Pro608=
XM_005246622.2:c.1602T>C	XP_005246679.1:p.Pro534=
XM_005246623.1:c.1602T>C	XP_005246680.1:p.Pro534=
XM_006712553.2:c.1749T>C	XP_006712616.1:p.Pro583=
XM_011511246.1:c.*25T>C	XP_011509548.1:n.*25T>C
NM_173173.2:c.1602T>C	NP_775265.1:p.Pro534=
XM_005246621.4:c.1824T>C	XP_005246678.1:p.Pro608=
XM_006712553.4:c.1749T>C	XP_006712616.1:p.Pro583=
XM_011511246.2:c.*25T>C	XP_011509548.1:n.*25T>C
XM_017004219.2:c.1791T>C	XP_016859708.1:p.Pro597=
XM_017004220.2:c.1716T>C	XP_016859709.1:p.Pro572=
XR_001738751.2:n.2038T>C
XR_001738752.2:n.1860T>C
XR_427087.4:n.1917T>C
NM_006186.4:c.1791T>C MANE Select	NP_006177.1:p.Pro597=
NM_173173.3:c.1602T>C	NP_775265.1:p.Pro534=