Canonical Allele Identifier: CA348679279

Gene: NR4A2

Linked Data

• MyVariant Identifiers: chr2:g.157182283T>A (hg19) ; chr2:g.156325771T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325771T>A , CM000664.2:g.156325771T>A	GRCh38
NC_000002.11:g.157182283T>A , CM000664.1:g.157182283T>A	GRCh37
NC_000002.10:g.156890529T>A	NCBI36
NG_011821.1:g.12005A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1566A>T	ENSP00000514865.1:p.Lys522Asn
ENST00000700229.1:c.734A>T
ENST00000700230.1:c.1310A>T	ENSP00000514867.1:n.1310A>T
ENST00000700231.1:c.1695A>T	ENSP00000514868.1:p.Lys565Asn
ENST00000339562.9:c.1770A>T MANE Select	ENSP00000344479.4:p.Lys590Asn
ENST00000675870.1:c.*281A>T	ENSP00000502739.1:n.*281A>T
ENST00000339562.8:c.1770A>T	ENSP00000344479.4:p.Lys590Asn
ENST00000409108.6:c.*4A>T	ENSP00000386993.2:n.*4A>T
ENST00000409572.5:c.1770A>T	ENSP00000386747.1:p.Lys590Asn
ENST00000417764.5:c.*281A>T	ENSP00000415632.1:n.*281A>T
ENST00000417972.5:c.*281A>T	ENSP00000394671.1:n.*281A>T
ENST00000426264.5:c.1581A>T	ENSP00000389986.1:p.Lys527Asn
ENST00000429376.5:c.*4A>T	ENSP00000410952.1:n.*4A>T
NM_006186.3:c.1770A>T	NP_006177.1:p.Lys590Asn
XM_005246621.2:c.1803A>T	XP_005246678.1:p.Lys601Asn
XM_005246622.2:c.1581A>T	XP_005246679.1:p.Lys527Asn
XM_005246623.1:c.1581A>T	XP_005246680.1:p.Lys527Asn
XM_006712553.2:c.1728A>T	XP_006712616.1:p.Lys576Asn
XM_011511246.1:c.*4A>T	XP_011509548.1:n.*4A>T
NM_173173.2:c.1581A>T	NP_775265.1:p.Lys527Asn
XM_005246621.4:c.1803A>T	XP_005246678.1:p.Lys601Asn
XM_006712553.4:c.1728A>T	XP_006712616.1:p.Lys576Asn
XM_011511246.2:c.*4A>T	XP_011509548.1:n.*4A>T
XM_017004219.2:c.1770A>T	XP_016859708.1:p.Lys590Asn
XM_017004220.2:c.1695A>T	XP_016859709.1:p.Lys565Asn
XR_001738751.2:n.2017A>T
XR_001738752.2:n.1839A>T
XR_427087.4:n.1896A>T
NM_006186.4:c.1770A>T MANE Select	NP_006177.1:p.Lys590Asn
NM_173173.3:c.1581A>T	NP_775265.1:p.Lys527Asn