Canonical Allele Identifier: CA348679762

Gene: NR4A2

Linked Data

• MyVariant Identifiers: chr2:g.157182459C>A (hg19) ; chr2:g.156325947C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325947C>A , CM000664.2:g.156325947C>A	GRCh38
NC_000002.11:g.157182459C>A , CM000664.1:g.157182459C>A	GRCh37
NC_000002.10:g.156890705C>A	NCBI36
NG_011821.1:g.11829G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1390G>T	ENSP00000514865.1:p.Val464Leu
ENST00000700229.1:c.558G>T
ENST00000700230.1:c.1134G>T	ENSP00000514867.1:n.1134G>T
ENST00000700231.1:c.1519G>T	ENSP00000514868.1:p.Val507Leu
ENST00000339562.9:c.1594G>T MANE Select	ENSP00000344479.4:p.Val532Leu
ENST00000675870.1:c.*105G>T	ENSP00000502739.1:n.*105G>T
ENST00000339562.8:c.1594G>T	ENSP00000344479.4:p.Val532Leu
ENST00000409108.6:c.1490G>T	ENSP00000386993.2:p.Cys497Phe
ENST00000409572.5:c.1594G>T	ENSP00000386747.1:p.Val532Leu
ENST00000417764.5:c.*105G>T	ENSP00000415632.1:n.*105G>T
ENST00000417972.5:c.*105G>T	ENSP00000394671.1:n.*105G>T
ENST00000426264.5:c.1405G>T	ENSP00000389986.1:p.Val469Leu
ENST00000429376.5:c.1301G>T	ENSP00000410952.1:p.Cys434Phe
NM_006186.3:c.1594G>T	NP_006177.1:p.Val532Leu
XM_005246621.2:c.1627G>T	XP_005246678.1:p.Val543Leu
XM_005246622.2:c.1405G>T	XP_005246679.1:p.Val469Leu
XM_005246623.1:c.1405G>T	XP_005246680.1:p.Val469Leu
XM_006712553.2:c.1552G>T	XP_006712616.1:p.Val518Leu
XM_011511246.1:c.1523G>T	XP_011509548.1:p.Cys508Phe
NM_173173.2:c.1405G>T	NP_775265.1:p.Val469Leu
XM_005246621.4:c.1627G>T	XP_005246678.1:p.Val543Leu
XM_006712553.4:c.1552G>T	XP_006712616.1:p.Val518Leu
XM_011511246.2:c.1523G>T	XP_011509548.1:p.Cys508Phe
XM_017004219.2:c.1594G>T	XP_016859708.1:p.Val532Leu
XM_017004220.2:c.1519G>T	XP_016859709.1:p.Val507Leu
XR_001738751.2:n.1841G>T
XR_001738752.2:n.1663G>T
XR_427087.4:n.1720G>T
NM_006186.4:c.1594G>T MANE Select	NP_006177.1:p.Val532Leu
NM_173173.3:c.1405G>T	NP_775265.1:p.Val469Leu