Canonical Allele Identifier: CA348679533

Gene: NR4A2

Linked Data

• MyVariant Identifiers: chr2:g.157182373T>C (hg19) ; chr2:g.156325861T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325861T>C , CM000664.2:g.156325861T>C	GRCh38
NC_000002.11:g.157182373T>C , CM000664.1:g.157182373T>C	GRCh37
NC_000002.10:g.156890619T>C	NCBI36
NG_011821.1:g.11915A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1476A>G	ENSP00000514865.1:p.Pro492=
ENST00000700229.1:c.644A>G
ENST00000700230.1:c.1220A>G	ENSP00000514867.1:n.1220A>G
ENST00000700231.1:c.1605A>G	ENSP00000514868.1:p.Pro535=
ENST00000339562.9:c.1680A>G MANE Select	ENSP00000344479.4:p.Pro560=
ENST00000675870.1:c.*191A>G	ENSP00000502739.1:n.*191A>G
ENST00000339562.8:c.1680A>G	ENSP00000344479.4:p.Pro560=
ENST00000409108.6:c.1576A>G	ENSP00000386993.2:p.Arg526Gly
ENST00000409572.5:c.1680A>G	ENSP00000386747.1:p.Pro560=
ENST00000417764.5:c.*191A>G	ENSP00000415632.1:n.*191A>G
ENST00000417972.5:c.*191A>G	ENSP00000394671.1:n.*191A>G
ENST00000426264.5:c.1491A>G	ENSP00000389986.1:p.Pro497=
ENST00000429376.5:c.1387A>G	ENSP00000410952.1:p.Arg463Gly
NM_006186.3:c.1680A>G	NP_006177.1:p.Pro560=
XM_005246621.2:c.1713A>G	XP_005246678.1:p.Pro571=
XM_005246622.2:c.1491A>G	XP_005246679.1:p.Pro497=
XM_005246623.1:c.1491A>G	XP_005246680.1:p.Pro497=
XM_006712553.2:c.1638A>G	XP_006712616.1:p.Pro546=
XM_011511246.1:c.1609A>G	XP_011509548.1:p.Arg537Gly
NM_173173.2:c.1491A>G	NP_775265.1:p.Pro497=
XM_005246621.4:c.1713A>G	XP_005246678.1:p.Pro571=
XM_006712553.4:c.1638A>G	XP_006712616.1:p.Pro546=
XM_011511246.2:c.1609A>G	XP_011509548.1:p.Arg537Gly
XM_017004219.2:c.1680A>G	XP_016859708.1:p.Pro560=
XM_017004220.2:c.1605A>G	XP_016859709.1:p.Pro535=
XR_001738751.2:n.1927A>G
XR_001738752.2:n.1749A>G
XR_427087.4:n.1806A>G
NM_006186.4:c.1680A>G MANE Select	NP_006177.1:p.Pro560=
NM_173173.3:c.1491A>G	NP_775265.1:p.Pro497=