Canonical Allele Identifier: CA348680059

Gene: NR4A2

Linked Data

• MyVariant Identifiers: chr2:g.157182711G>A (hg19) ; chr2:g.156326199G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156326199G>A , CM000664.2:g.156326199G>A	GRCh38
NC_000002.11:g.157182711G>A , CM000664.1:g.157182711G>A	GRCh37
NC_000002.10:g.156890957G>A	NCBI36
NG_011821.1:g.11577C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1287C>T	ENSP00000514865.1:p.Asn429=
ENST00000700229.1:c.455C>T
ENST00000700230.1:c.1031C>T	ENSP00000514867.1:n.1031C>T
ENST00000700231.1:c.1416C>T	ENSP00000514868.1:p.Asn472=
ENST00000339562.9:c.1491C>T MANE Select	ENSP00000344479.4:p.Asn497=
ENST00000675870.1:c.*2C>T	ENSP00000502739.1:n.*2C>T
ENST00000339562.8:c.1491C>T	ENSP00000344479.4:p.Asn497=
ENST00000409108.6:c.1387C>T	ENSP00000386993.2:p.His463Tyr
ENST00000409572.5:c.1491C>T	ENSP00000386747.1:p.Asn497=
ENST00000417764.5:c.*2C>T	ENSP00000415632.1:n.*2C>T
ENST00000417972.5:c.*2C>T	ENSP00000394671.1:n.*2C>T
ENST00000426264.5:c.1302C>T	ENSP00000389986.1:p.Asn434=
ENST00000429376.5:c.1198C>T	ENSP00000410952.1:p.His400Tyr
NM_006186.3:c.1491C>T	NP_006177.1:p.Asn497=
XM_005246621.2:c.1524C>T	XP_005246678.1:p.Asn508=
XM_005246622.2:c.1302C>T	XP_005246679.1:p.Asn434=
XM_005246623.1:c.1302C>T	XP_005246680.1:p.Asn434=
XM_006712553.2:c.1449C>T	XP_006712616.1:p.Asn483=
XM_011511246.1:c.1420C>T	XP_011509548.1:p.His474Tyr
XR_427087.2:n.3576C>T
NM_173173.2:c.1302C>T	NP_775265.1:p.Asn434=
XM_005246621.4:c.1524C>T	XP_005246678.1:p.Asn508=
XM_006712553.4:c.1449C>T	XP_006712616.1:p.Asn483=
XM_011511246.2:c.1420C>T	XP_011509548.1:p.His474Tyr
XM_017004219.2:c.1491C>T	XP_016859708.1:p.Asn497=
XM_017004220.2:c.1416C>T	XP_016859709.1:p.Asn472=
XR_001738751.2:n.1738C>T
XR_001738752.2:n.1560C>T
XR_427087.4:n.1617C>T
NM_006186.4:c.1491C>T MANE Select	NP_006177.1:p.Asn497=
NM_173173.3:c.1302C>T	NP_775265.1:p.Asn434=