Canonical Allele Identifier: CA348680017

Gene: NR4A2

Linked Data

• MyVariant Identifiers: chr2:g.157182695A>C (hg19) ; chr2:g.156326183A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156326183A>C , CM000664.2:g.156326183A>C	GRCh38
NC_000002.11:g.157182695A>C , CM000664.1:g.157182695A>C	GRCh37
NC_000002.10:g.156890941A>C	NCBI36
NG_011821.1:g.11593T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1303T>G	ENSP00000514865.1:p.Phe435Val
ENST00000700229.1:c.471T>G
ENST00000700230.1:c.1047T>G	ENSP00000514867.1:n.1047T>G
ENST00000700231.1:c.1432T>G	ENSP00000514868.1:p.Phe478Val
ENST00000339562.9:c.1507T>G MANE Select	ENSP00000344479.4:p.Phe503Val
ENST00000675870.1:c.*18T>G	ENSP00000502739.1:n.*18T>G
ENST00000339562.8:c.1507T>G	ENSP00000344479.4:p.Phe503Val
ENST00000409108.6:c.1403T>G	ENSP00000386993.2:p.Leu468Arg
ENST00000409572.5:c.1507T>G	ENSP00000386747.1:p.Phe503Val
ENST00000417764.5:c.*18T>G	ENSP00000415632.1:n.*18T>G
ENST00000417972.5:c.*18T>G	ENSP00000394671.1:n.*18T>G
ENST00000426264.5:c.1318T>G	ENSP00000389986.1:p.Phe440Val
ENST00000429376.5:c.1214T>G	ENSP00000410952.1:p.Leu405Arg
NM_006186.3:c.1507T>G	NP_006177.1:p.Phe503Val
XM_005246621.2:c.1540T>G	XP_005246678.1:p.Phe514Val
XM_005246622.2:c.1318T>G	XP_005246679.1:p.Phe440Val
XM_005246623.1:c.1318T>G	XP_005246680.1:p.Phe440Val
XM_006712553.2:c.1465T>G	XP_006712616.1:p.Phe489Val
XM_011511246.1:c.1436T>G	XP_011509548.1:p.Leu479Arg
XR_427087.2:n.3592T>G
NM_173173.2:c.1318T>G	NP_775265.1:p.Phe440Val
XM_005246621.4:c.1540T>G	XP_005246678.1:p.Phe514Val
XM_006712553.4:c.1465T>G	XP_006712616.1:p.Phe489Val
XM_011511246.2:c.1436T>G	XP_011509548.1:p.Leu479Arg
XM_017004219.2:c.1507T>G	XP_016859708.1:p.Phe503Val
XM_017004220.2:c.1432T>G	XP_016859709.1:p.Phe478Val
XR_001738751.2:n.1754T>G
XR_001738752.2:n.1576T>G
XR_427087.4:n.1633T>G
NM_006186.4:c.1507T>G MANE Select	NP_006177.1:p.Phe503Val
NM_173173.3:c.1318T>G	NP_775265.1:p.Phe440Val