Canonical Allele Identifier: CA348679700

Gene: NR4A2

Linked Data

• MyVariant Identifiers: chr2:g.157182436C>T (hg19) ; chr2:g.156325924C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325924C>T , CM000664.2:g.156325924C>T	GRCh38
NC_000002.11:g.157182436C>T , CM000664.1:g.157182436C>T	GRCh37
NC_000002.10:g.156890682C>T	NCBI36
NG_011821.1:g.11852G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1413G>A	ENSP00000514865.1:p.Val471=
ENST00000700229.1:c.581G>A
ENST00000700230.1:c.1157G>A	ENSP00000514867.1:n.1157G>A
ENST00000700231.1:c.1542G>A	ENSP00000514868.1:p.Val514=
ENST00000339562.9:c.1617G>A MANE Select	ENSP00000344479.4:p.Val539=
ENST00000675870.1:c.*128G>A	ENSP00000502739.1:n.*128G>A
ENST00000339562.8:c.1617G>A	ENSP00000344479.4:p.Val539=
ENST00000409108.6:c.1513G>A	ENSP00000386993.2:p.Asp505Asn
ENST00000409572.5:c.1617G>A	ENSP00000386747.1:p.Val539=
ENST00000417764.5:c.*128G>A	ENSP00000415632.1:n.*128G>A
ENST00000417972.5:c.*128G>A	ENSP00000394671.1:n.*128G>A
ENST00000426264.5:c.1428G>A	ENSP00000389986.1:p.Val476=
ENST00000429376.5:c.1324G>A	ENSP00000410952.1:p.Asp442Asn
NM_006186.3:c.1617G>A	NP_006177.1:p.Val539=
XM_005246621.2:c.1650G>A	XP_005246678.1:p.Val550=
XM_005246622.2:c.1428G>A	XP_005246679.1:p.Val476=
XM_005246623.1:c.1428G>A	XP_005246680.1:p.Val476=
XM_006712553.2:c.1575G>A	XP_006712616.1:p.Val525=
XM_011511246.1:c.1546G>A	XP_011509548.1:p.Asp516Asn
NM_173173.2:c.1428G>A	NP_775265.1:p.Val476=
XM_005246621.4:c.1650G>A	XP_005246678.1:p.Val550=
XM_006712553.4:c.1575G>A	XP_006712616.1:p.Val525=
XM_011511246.2:c.1546G>A	XP_011509548.1:p.Asp516Asn
XM_017004219.2:c.1617G>A	XP_016859708.1:p.Val539=
XM_017004220.2:c.1542G>A	XP_016859709.1:p.Val514=
XR_001738751.2:n.1864G>A
XR_001738752.2:n.1686G>A
XR_427087.4:n.1743G>A
NM_006186.4:c.1617G>A MANE Select	NP_006177.1:p.Val539=
NM_173173.3:c.1428G>A	NP_775265.1:p.Val476=