Canonical Allele Identifier: CA429586156

Gene: NR4A2

Linked Data

• MyVariant Identifiers: chr2:g.157182259G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325747G>A , CM000664.2:g.156325747G>A	GRCh38
NC_000002.11:g.157182259G>A , CM000664.1:g.157182259G>A	GRCh37
NC_000002.10:g.156890505G>A	NCBI36
NG_011821.1:g.12029C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1590C>T	ENSP00000514865.1:p.Phe530=
ENST00000700229.1:c.758C>T
ENST00000700230.1:c.1334C>T	ENSP00000514867.1:n.1334C>T
ENST00000700231.1:c.1719C>T	ENSP00000514868.1:p.Phe573=
ENST00000339562.9:c.1794C>T MANE Select	ENSP00000344479.4:p.Phe598=
ENST00000675870.1:c.*305C>T	ENSP00000502739.1:n.*305C>T
ENST00000339562.8:c.1794C>T	ENSP00000344479.4:p.Phe598=
ENST00000409108.6:c.*28C>T	ENSP00000386993.2:n.*28C>T
ENST00000409572.5:c.1794C>T	ENSP00000386747.1:p.Phe598=
ENST00000417764.5:c.*305C>T	ENSP00000415632.1:n.*305C>T
ENST00000417972.5:c.*305C>T	ENSP00000394671.1:n.*305C>T
ENST00000426264.5:c.1605C>T	ENSP00000389986.1:p.Phe535=
ENST00000429376.5:c.*28C>T	ENSP00000410952.1:n.*28C>T
NM_006186.3:c.1794C>T	NP_006177.1:p.Phe598=
XM_005246621.2:c.1827C>T	XP_005246678.1:p.Phe609=
XM_005246622.2:c.1605C>T	XP_005246679.1:p.Phe535=
XM_005246623.1:c.1605C>T	XP_005246680.1:p.Phe535=
XM_006712553.2:c.1752C>T	XP_006712616.1:p.Phe584=
XM_011511246.1:c.*28C>T	XP_011509548.1:n.*28C>T
NM_173173.2:c.1605C>T	NP_775265.1:p.Phe535=
XM_005246621.4:c.1827C>T	XP_005246678.1:p.Phe609=
XM_006712553.4:c.1752C>T	XP_006712616.1:p.Phe584=
XM_011511246.2:c.*28C>T	XP_011509548.1:n.*28C>T
XM_017004219.2:c.1794C>T	XP_016859708.1:p.Phe598=
XM_017004220.2:c.1719C>T	XP_016859709.1:p.Phe573=
XR_001738751.2:n.2041C>T
XR_001738752.2:n.1863C>T
XR_427087.4:n.1920C>T
NM_006186.4:c.1794C>T MANE Select	NP_006177.1:p.Phe598=
NM_173173.3:c.1605C>T	NP_775265.1:p.Phe535=