Canonical Allele Identifier: CA348679746

Gene: NR4A2

Linked Data

• MyVariant Identifiers: chr2:g.157182453A>G (hg19) ; chr2:g.156325941A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325941A>G , CM000664.2:g.156325941A>G	GRCh38
NC_000002.11:g.157182453A>G , CM000664.1:g.157182453A>G	GRCh37
NC_000002.10:g.156890699A>G	NCBI36
NG_011821.1:g.11835T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1396T>C	ENSP00000514865.1:p.Cys466Arg
ENST00000700229.1:c.564T>C
ENST00000700230.1:c.1140T>C	ENSP00000514867.1:n.1140T>C
ENST00000700231.1:c.1525T>C	ENSP00000514868.1:p.Cys509Arg
ENST00000339562.9:c.1600T>C MANE Select	ENSP00000344479.4:p.Cys534Arg
ENST00000675870.1:c.*111T>C	ENSP00000502739.1:n.*111T>C
ENST00000339562.8:c.1600T>C	ENSP00000344479.4:p.Cys534Arg
ENST00000409108.6:c.1496T>C	ENSP00000386993.2:p.Leu499Ser
ENST00000409572.5:c.1600T>C	ENSP00000386747.1:p.Cys534Arg
ENST00000417764.5:c.*111T>C	ENSP00000415632.1:n.*111T>C
ENST00000417972.5:c.*111T>C	ENSP00000394671.1:n.*111T>C
ENST00000426264.5:c.1411T>C	ENSP00000389986.1:p.Cys471Arg
ENST00000429376.5:c.1307T>C	ENSP00000410952.1:p.Leu436Ser
NM_006186.3:c.1600T>C	NP_006177.1:p.Cys534Arg
XM_005246621.2:c.1633T>C	XP_005246678.1:p.Cys545Arg
XM_005246622.2:c.1411T>C	XP_005246679.1:p.Cys471Arg
XM_005246623.1:c.1411T>C	XP_005246680.1:p.Cys471Arg
XM_006712553.2:c.1558T>C	XP_006712616.1:p.Cys520Arg
XM_011511246.1:c.1529T>C	XP_011509548.1:p.Leu510Ser
NM_173173.2:c.1411T>C	NP_775265.1:p.Cys471Arg
XM_005246621.4:c.1633T>C	XP_005246678.1:p.Cys545Arg
XM_006712553.4:c.1558T>C	XP_006712616.1:p.Cys520Arg
XM_011511246.2:c.1529T>C	XP_011509548.1:p.Leu510Ser
XM_017004219.2:c.1600T>C	XP_016859708.1:p.Cys534Arg
XM_017004220.2:c.1525T>C	XP_016859709.1:p.Cys509Arg
XR_001738751.2:n.1847T>C
XR_001738752.2:n.1669T>C
XR_427087.4:n.1726T>C
NM_006186.4:c.1600T>C MANE Select	NP_006177.1:p.Cys534Arg
NM_173173.3:c.1411T>C	NP_775265.1:p.Cys471Arg