Canonical Allele Identifier: CA348679984

Gene: NR4A2

Linked Data

• MyVariant Identifiers: chr2:g.157182682G>T (hg19) ; chr2:g.156326170G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156326170G>T , CM000664.2:g.156326170G>T	GRCh38
NC_000002.11:g.157182682G>T , CM000664.1:g.157182682G>T	GRCh37
NC_000002.10:g.156890928G>T	NCBI36
NG_011821.1:g.11606C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1316C>A	ENSP00000514865.1:p.Ala439Asp
ENST00000700229.1:c.484C>A
ENST00000700230.1:c.1060C>A	ENSP00000514867.1:n.1060C>A
ENST00000700231.1:c.1445C>A	ENSP00000514868.1:p.Ala482Asp
ENST00000339562.9:c.1520C>A MANE Select	ENSP00000344479.4:p.Ala507Asp
ENST00000675870.1:c.*31C>A	ENSP00000502739.1:n.*31C>A
ENST00000339562.8:c.1520C>A	ENSP00000344479.4:p.Ala507Asp
ENST00000409108.6:c.1416C>A	ENSP00000386993.2:p.Cys472Ter
ENST00000409572.5:c.1520C>A	ENSP00000386747.1:p.Ala507Asp
ENST00000417764.5:c.*31C>A	ENSP00000415632.1:n.*31C>A
ENST00000417972.5:c.*31C>A	ENSP00000394671.1:n.*31C>A
ENST00000426264.5:c.1331C>A	ENSP00000389986.1:p.Ala444Asp
ENST00000429376.5:c.1227C>A	ENSP00000410952.1:p.Cys409Ter
NM_006186.3:c.1520C>A	NP_006177.1:p.Ala507Asp
XM_005246621.2:c.1553C>A	XP_005246678.1:p.Ala518Asp
XM_005246622.2:c.1331C>A	XP_005246679.1:p.Ala444Asp
XM_005246623.1:c.1331C>A	XP_005246680.1:p.Ala444Asp
XM_006712553.2:c.1478C>A	XP_006712616.1:p.Ala493Asp
XM_011511246.1:c.1449C>A	XP_011509548.1:p.Cys483Ter
XR_427087.2:n.3605C>A
NM_173173.2:c.1331C>A	NP_775265.1:p.Ala444Asp
XM_005246621.4:c.1553C>A	XP_005246678.1:p.Ala518Asp
XM_006712553.4:c.1478C>A	XP_006712616.1:p.Ala493Asp
XM_011511246.2:c.1449C>A	XP_011509548.1:p.Cys483Ter
XM_017004219.2:c.1520C>A	XP_016859708.1:p.Ala507Asp
XM_017004220.2:c.1445C>A	XP_016859709.1:p.Ala482Asp
XR_001738751.2:n.1767C>A
XR_001738752.2:n.1589C>A
XR_427087.4:n.1646C>A
NM_006186.4:c.1520C>A MANE Select	NP_006177.1:p.Ala507Asp
NM_173173.3:c.1331C>A	NP_775265.1:p.Ala444Asp