Canonical Allele Identifier: CA348679318

Gene: NR4A2

Linked Data

• COSMIC: COSM476053
• MyVariant Identifiers: chr2:g.157182297C>T (hg19) ; chr2:g.156325785C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325785C>T , CM000664.2:g.156325785C>T	GRCh38
NC_000002.11:g.157182297C>T , CM000664.1:g.157182297C>T	GRCh37
NC_000002.10:g.156890543C>T	NCBI36
NG_011821.1:g.11991G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1552G>A	ENSP00000514865.1:p.Ala518Thr
ENST00000700229.1:c.720G>A
ENST00000700230.1:c.1296G>A	ENSP00000514867.1:n.1296G>A
ENST00000700231.1:c.1681G>A	ENSP00000514868.1:p.Ala561Thr
ENST00000339562.9:c.1756G>A MANE Select	ENSP00000344479.4:p.Ala586Thr
ENST00000675870.1:c.*267G>A	ENSP00000502739.1:n.*267G>A
ENST00000339562.8:c.1756G>A	ENSP00000344479.4:p.Ala586Thr
ENST00000409108.6:c.1652G>A	ENSP00000386993.2:p.Ser551Asn
ENST00000409572.5:c.1756G>A	ENSP00000386747.1:p.Ala586Thr
ENST00000417764.5:c.*267G>A	ENSP00000415632.1:n.*267G>A
ENST00000417972.5:c.*267G>A	ENSP00000394671.1:n.*267G>A
ENST00000426264.5:c.1567G>A	ENSP00000389986.1:p.Ala523Thr
ENST00000429376.5:c.1463G>A	ENSP00000410952.1:p.Ser488Asn
NM_006186.3:c.1756G>A	NP_006177.1:p.Ala586Thr
XM_005246621.2:c.1789G>A	XP_005246678.1:p.Ala597Thr
XM_005246622.2:c.1567G>A	XP_005246679.1:p.Ala523Thr
XM_005246623.1:c.1567G>A	XP_005246680.1:p.Ala523Thr
XM_006712553.2:c.1714G>A	XP_006712616.1:p.Ala572Thr
XM_011511246.1:c.1685G>A	XP_011509548.1:p.Ser562Asn
NM_173173.2:c.1567G>A	NP_775265.1:p.Ala523Thr
XM_005246621.4:c.1789G>A	XP_005246678.1:p.Ala597Thr
XM_006712553.4:c.1714G>A	XP_006712616.1:p.Ala572Thr
XM_011511246.2:c.1685G>A	XP_011509548.1:p.Ser562Asn
XM_017004219.2:c.1756G>A	XP_016859708.1:p.Ala586Thr
XM_017004220.2:c.1681G>A	XP_016859709.1:p.Ala561Thr
XR_001738751.2:n.2003G>A
XR_001738752.2:n.1825G>A
XR_427087.4:n.1882G>A
NM_006186.4:c.1756G>A MANE Select	NP_006177.1:p.Ala586Thr
NM_173173.3:c.1567G>A	NP_775265.1:p.Ala523Thr