Canonical Allele Identifier: CA348679790

Gene: NR4A2

Linked Data

• MyVariant Identifiers: chr2:g.157182468T>G (hg19) ; chr2:g.156325956T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325956T>G , CM000664.2:g.156325956T>G	GRCh38
NC_000002.11:g.157182468T>G , CM000664.1:g.157182468T>G	GRCh37
NC_000002.10:g.156890714T>G	NCBI36
NG_011821.1:g.11820A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1381A>C	ENSP00000514865.1:p.Asn461His
ENST00000700229.1:c.549A>C
ENST00000700230.1:c.1125A>C	ENSP00000514867.1:n.1125A>C
ENST00000700231.1:c.1510A>C	ENSP00000514868.1:p.Asn504His
ENST00000339562.9:c.1585A>C MANE Select	ENSP00000344479.4:p.Asn529His
ENST00000675870.1:c.*96A>C	ENSP00000502739.1:n.*96A>C
ENST00000339562.8:c.1585A>C	ENSP00000344479.4:p.Asn529His
ENST00000409108.6:c.1481A>C	ENSP00000386993.2:p.Lys494Thr
ENST00000409572.5:c.1585A>C	ENSP00000386747.1:p.Asn529His
ENST00000417764.5:c.*96A>C	ENSP00000415632.1:n.*96A>C
ENST00000417972.5:c.*96A>C	ENSP00000394671.1:n.*96A>C
ENST00000426264.5:c.1396A>C	ENSP00000389986.1:p.Asn466His
ENST00000429376.5:c.1292A>C	ENSP00000410952.1:p.Lys431Thr
NM_006186.3:c.1585A>C	NP_006177.1:p.Asn529His
XM_005246621.2:c.1618A>C	XP_005246678.1:p.Asn540His
XM_005246622.2:c.1396A>C	XP_005246679.1:p.Asn466His
XM_005246623.1:c.1396A>C	XP_005246680.1:p.Asn466His
XM_006712553.2:c.1543A>C	XP_006712616.1:p.Asn515His
XM_011511246.1:c.1514A>C	XP_011509548.1:p.Lys505Thr
NM_173173.2:c.1396A>C	NP_775265.1:p.Asn466His
XM_005246621.4:c.1618A>C	XP_005246678.1:p.Asn540His
XM_006712553.4:c.1543A>C	XP_006712616.1:p.Asn515His
XM_011511246.2:c.1514A>C	XP_011509548.1:p.Lys505Thr
XM_017004219.2:c.1585A>C	XP_016859708.1:p.Asn529His
XM_017004220.2:c.1510A>C	XP_016859709.1:p.Asn504His
XR_001738751.2:n.1832A>C
XR_001738752.2:n.1654A>C
XR_427087.4:n.1711A>C
NM_006186.4:c.1585A>C MANE Select	NP_006177.1:p.Asn529His
NM_173173.3:c.1396A>C	NP_775265.1:p.Asn466His