Canonical Allele Identifier: CA348679831

Gene: NR4A2

Linked Data

• MyVariant Identifiers: chr2:g.157182482A>T (hg19) ; chr2:g.156325970A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325970A>T , CM000664.2:g.156325970A>T	GRCh38
NC_000002.11:g.157182482A>T , CM000664.1:g.157182482A>T	GRCh37
NC_000002.10:g.156890728A>T	NCBI36
NG_011821.1:g.11806T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1367T>A	ENSP00000514865.1:p.Val456Glu
ENST00000700229.1:c.535T>A
ENST00000700230.1:c.1111T>A	ENSP00000514867.1:n.1111T>A
ENST00000700231.1:c.1496T>A	ENSP00000514868.1:p.Val499Glu
ENST00000339562.9:c.1571T>A MANE Select	ENSP00000344479.4:p.Val524Glu
ENST00000675870.1:c.*82T>A	ENSP00000502739.1:n.*82T>A
ENST00000339562.8:c.1571T>A	ENSP00000344479.4:p.Val524Glu
ENST00000409108.6:c.1467T>A	ENSP00000386993.2:p.Ser489Arg
ENST00000409572.5:c.1571T>A	ENSP00000386747.1:p.Val524Glu
ENST00000417764.5:c.*82T>A	ENSP00000415632.1:n.*82T>A
ENST00000417972.5:c.*82T>A	ENSP00000394671.1:n.*82T>A
ENST00000426264.5:c.1382T>A	ENSP00000389986.1:p.Val461Glu
ENST00000429376.5:c.1278T>A	ENSP00000410952.1:p.Ser426Arg
NM_006186.3:c.1571T>A	NP_006177.1:p.Val524Glu
XM_005246621.2:c.1604T>A	XP_005246678.1:p.Val535Glu
XM_005246622.2:c.1382T>A	XP_005246679.1:p.Val461Glu
XM_005246623.1:c.1382T>A	XP_005246680.1:p.Val461Glu
XM_006712553.2:c.1529T>A	XP_006712616.1:p.Val510Glu
XM_011511246.1:c.1500T>A	XP_011509548.1:p.Ser500Arg
XR_427087.2:n.3656T>A
NM_173173.2:c.1382T>A	NP_775265.1:p.Val461Glu
XM_005246621.4:c.1604T>A	XP_005246678.1:p.Val535Glu
XM_006712553.4:c.1529T>A	XP_006712616.1:p.Val510Glu
XM_011511246.2:c.1500T>A	XP_011509548.1:p.Ser500Arg
XM_017004219.2:c.1571T>A	XP_016859708.1:p.Val524Glu
XM_017004220.2:c.1496T>A	XP_016859709.1:p.Val499Glu
XR_001738751.2:n.1818T>A
XR_001738752.2:n.1640T>A
XR_427087.4:n.1697T>A
NM_006186.4:c.1571T>A MANE Select	NP_006177.1:p.Val524Glu
NM_173173.3:c.1382T>A	NP_775265.1:p.Val461Glu