Canonical Allele Identifier: CA348679734

Gene: NR4A2

Linked Data

• MyVariant Identifiers: chr2:g.157182449A>C (hg19) ; chr2:g.156325937A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325937A>C , CM000664.2:g.156325937A>C	GRCh38
NC_000002.11:g.157182449A>C , CM000664.1:g.157182449A>C	GRCh37
NC_000002.10:g.156890695A>C	NCBI36
NG_011821.1:g.11839T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1400T>G	ENSP00000514865.1:p.Leu467Arg
ENST00000700229.1:c.568T>G
ENST00000700230.1:c.1144T>G	ENSP00000514867.1:n.1144T>G
ENST00000700231.1:c.1529T>G	ENSP00000514868.1:p.Leu510Arg
ENST00000339562.9:c.1604T>G MANE Select	ENSP00000344479.4:p.Leu535Arg
ENST00000675870.1:c.*115T>G	ENSP00000502739.1:n.*115T>G
ENST00000339562.8:c.1604T>G	ENSP00000344479.4:p.Leu535Arg
ENST00000409108.6:c.1500T>G	ENSP00000386993.2:p.Ser500=
ENST00000409572.5:c.1604T>G	ENSP00000386747.1:p.Leu535Arg
ENST00000417764.5:c.*115T>G	ENSP00000415632.1:n.*115T>G
ENST00000417972.5:c.*115T>G	ENSP00000394671.1:n.*115T>G
ENST00000426264.5:c.1415T>G	ENSP00000389986.1:p.Leu472Arg
ENST00000429376.5:c.1311T>G	ENSP00000410952.1:p.Ser437=
NM_006186.3:c.1604T>G	NP_006177.1:p.Leu535Arg
XM_005246621.2:c.1637T>G	XP_005246678.1:p.Leu546Arg
XM_005246622.2:c.1415T>G	XP_005246679.1:p.Leu472Arg
XM_005246623.1:c.1415T>G	XP_005246680.1:p.Leu472Arg
XM_006712553.2:c.1562T>G	XP_006712616.1:p.Leu521Arg
XM_011511246.1:c.1533T>G	XP_011509548.1:p.Ser511=
NM_173173.2:c.1415T>G	NP_775265.1:p.Leu472Arg
XM_005246621.4:c.1637T>G	XP_005246678.1:p.Leu546Arg
XM_006712553.4:c.1562T>G	XP_006712616.1:p.Leu521Arg
XM_011511246.2:c.1533T>G	XP_011509548.1:p.Ser511=
XM_017004219.2:c.1604T>G	XP_016859708.1:p.Leu535Arg
XM_017004220.2:c.1529T>G	XP_016859709.1:p.Leu510Arg
XR_001738751.2:n.1851T>G
XR_001738752.2:n.1673T>G
XR_427087.4:n.1730T>G
NM_006186.4:c.1604T>G MANE Select	NP_006177.1:p.Leu535Arg
NM_173173.3:c.1415T>G	NP_775265.1:p.Leu472Arg