Canonical Allele Identifier: CA348679466

Gene: NR4A2

Linked Data

• MyVariant Identifiers: chr2:g.157182349C>T (hg19) ; chr2:g.156325837C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325837C>T , CM000664.2:g.156325837C>T	GRCh38
NC_000002.11:g.157182349C>T , CM000664.1:g.157182349C>T	GRCh37
NC_000002.10:g.156890595C>T	NCBI36
NG_011821.1:g.11939G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1500G>A	ENSP00000514865.1:p.Gln500=
ENST00000700229.1:c.668G>A
ENST00000700230.1:c.1244G>A	ENSP00000514867.1:n.1244G>A
ENST00000700231.1:c.1629G>A	ENSP00000514868.1:p.Gln543=
ENST00000339562.9:c.1704G>A MANE Select	ENSP00000344479.4:p.Gln568=
ENST00000675870.1:c.*215G>A	ENSP00000502739.1:n.*215G>A
ENST00000339562.8:c.1704G>A	ENSP00000344479.4:p.Gln568=
ENST00000409108.6:c.1600G>A	ENSP00000386993.2:p.Gly534Arg
ENST00000409572.5:c.1704G>A	ENSP00000386747.1:p.Gln568=
ENST00000417764.5:c.*215G>A	ENSP00000415632.1:n.*215G>A
ENST00000417972.5:c.*215G>A	ENSP00000394671.1:n.*215G>A
ENST00000426264.5:c.1515G>A	ENSP00000389986.1:p.Gln505=
ENST00000429376.5:c.1411G>A	ENSP00000410952.1:p.Gly471Arg
NM_006186.3:c.1704G>A	NP_006177.1:p.Gln568=
XM_005246621.2:c.1737G>A	XP_005246678.1:p.Gln579=
XM_005246622.2:c.1515G>A	XP_005246679.1:p.Gln505=
XM_005246623.1:c.1515G>A	XP_005246680.1:p.Gln505=
XM_006712553.2:c.1662G>A	XP_006712616.1:p.Gln554=
XM_011511246.1:c.1633G>A	XP_011509548.1:p.Gly545Arg
NM_173173.2:c.1515G>A	NP_775265.1:p.Gln505=
XM_005246621.4:c.1737G>A	XP_005246678.1:p.Gln579=
XM_006712553.4:c.1662G>A	XP_006712616.1:p.Gln554=
XM_011511246.2:c.1633G>A	XP_011509548.1:p.Gly545Arg
XM_017004219.2:c.1704G>A	XP_016859708.1:p.Gln568=
XM_017004220.2:c.1629G>A	XP_016859709.1:p.Gln543=
XR_001738751.2:n.1951G>A
XR_001738752.2:n.1773G>A
XR_427087.4:n.1830G>A
NM_006186.4:c.1704G>A MANE Select	NP_006177.1:p.Gln568=
NM_173173.3:c.1515G>A	NP_775265.1:p.Gln505=