Canonical Allele Identifier: CA348679987

Gene: NR4A2

Linked Data

• gnomAD v4: 2-156326171-C-T
• MyVariant Identifiers: chr2:g.157182683C>T (hg19) ; chr2:g.156326171C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156326171C>T , CM000664.2:g.156326171C>T	GRCh38
NC_000002.11:g.157182683C>T , CM000664.1:g.157182683C>T	GRCh37
NC_000002.10:g.156890929C>T	NCBI36
NG_011821.1:g.11605G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1315G>A	ENSP00000514865.1:p.Ala439Thr
ENST00000700229.1:c.483G>A
ENST00000700230.1:c.1059G>A	ENSP00000514867.1:n.1059G>A
ENST00000700231.1:c.1444G>A	ENSP00000514868.1:p.Ala482Thr
ENST00000339562.9:c.1519G>A MANE Select	ENSP00000344479.4:p.Ala507Thr
ENST00000675870.1:c.*30G>A	ENSP00000502739.1:n.*30G>A
ENST00000339562.8:c.1519G>A	ENSP00000344479.4:p.Ala507Thr
ENST00000409108.6:c.1415G>A	ENSP00000386993.2:p.Cys472Tyr
ENST00000409572.5:c.1519G>A	ENSP00000386747.1:p.Ala507Thr
ENST00000417764.5:c.*30G>A	ENSP00000415632.1:n.*30G>A
ENST00000417972.5:c.*30G>A	ENSP00000394671.1:n.*30G>A
ENST00000426264.5:c.1330G>A	ENSP00000389986.1:p.Ala444Thr
ENST00000429376.5:c.1226G>A	ENSP00000410952.1:p.Cys409Tyr
NM_006186.3:c.1519G>A	NP_006177.1:p.Ala507Thr
XM_005246621.2:c.1552G>A	XP_005246678.1:p.Ala518Thr
XM_005246622.2:c.1330G>A	XP_005246679.1:p.Ala444Thr
XM_005246623.1:c.1330G>A	XP_005246680.1:p.Ala444Thr
XM_006712553.2:c.1477G>A	XP_006712616.1:p.Ala493Thr
XM_011511246.1:c.1448G>A	XP_011509548.1:p.Cys483Tyr
XR_427087.2:n.3604G>A
NM_173173.2:c.1330G>A	NP_775265.1:p.Ala444Thr
XM_005246621.4:c.1552G>A	XP_005246678.1:p.Ala518Thr
XM_006712553.4:c.1477G>A	XP_006712616.1:p.Ala493Thr
XM_011511246.2:c.1448G>A	XP_011509548.1:p.Cys483Tyr
XM_017004219.2:c.1519G>A	XP_016859708.1:p.Ala507Thr
XM_017004220.2:c.1444G>A	XP_016859709.1:p.Ala482Thr
XR_001738751.2:n.1766G>A
XR_001738752.2:n.1588G>A
XR_427087.4:n.1645G>A
NM_006186.4:c.1519G>A MANE Select	NP_006177.1:p.Ala507Thr
NM_173173.3:c.1330G>A	NP_775265.1:p.Ala444Thr