Canonical Allele Identifier: CA348679758

Gene: NR4A2

Linked Data

• MyVariant Identifiers: chr2:g.157182458A>C (hg19) ; chr2:g.156325946A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325946A>C , CM000664.2:g.156325946A>C	GRCh38
NC_000002.11:g.157182458A>C , CM000664.1:g.157182458A>C	GRCh37
NC_000002.10:g.156890704A>C	NCBI36
NG_011821.1:g.11830T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1391T>G	ENSP00000514865.1:p.Val464Gly
ENST00000700229.1:c.559T>G
ENST00000700230.1:c.1135T>G	ENSP00000514867.1:n.1135T>G
ENST00000700231.1:c.1520T>G	ENSP00000514868.1:p.Val507Gly
ENST00000339562.9:c.1595T>G MANE Select	ENSP00000344479.4:p.Val532Gly
ENST00000675870.1:c.*106T>G	ENSP00000502739.1:n.*106T>G
ENST00000339562.8:c.1595T>G	ENSP00000344479.4:p.Val532Gly
ENST00000409108.6:c.1491T>G	ENSP00000386993.2:p.Cys497Trp
ENST00000409572.5:c.1595T>G	ENSP00000386747.1:p.Val532Gly
ENST00000417764.5:c.*106T>G	ENSP00000415632.1:n.*106T>G
ENST00000417972.5:c.*106T>G	ENSP00000394671.1:n.*106T>G
ENST00000426264.5:c.1406T>G	ENSP00000389986.1:p.Val469Gly
ENST00000429376.5:c.1302T>G	ENSP00000410952.1:p.Cys434Trp
NM_006186.3:c.1595T>G	NP_006177.1:p.Val532Gly
XM_005246621.2:c.1628T>G	XP_005246678.1:p.Val543Gly
XM_005246622.2:c.1406T>G	XP_005246679.1:p.Val469Gly
XM_005246623.1:c.1406T>G	XP_005246680.1:p.Val469Gly
XM_006712553.2:c.1553T>G	XP_006712616.1:p.Val518Gly
XM_011511246.1:c.1524T>G	XP_011509548.1:p.Cys508Trp
NM_173173.2:c.1406T>G	NP_775265.1:p.Val469Gly
XM_005246621.4:c.1628T>G	XP_005246678.1:p.Val543Gly
XM_006712553.4:c.1553T>G	XP_006712616.1:p.Val518Gly
XM_011511246.2:c.1524T>G	XP_011509548.1:p.Cys508Trp
XM_017004219.2:c.1595T>G	XP_016859708.1:p.Val532Gly
XM_017004220.2:c.1520T>G	XP_016859709.1:p.Val507Gly
XR_001738751.2:n.1842T>G
XR_001738752.2:n.1664T>G
XR_427087.4:n.1721T>G
NM_006186.4:c.1595T>G MANE Select	NP_006177.1:p.Val532Gly
NM_173173.3:c.1406T>G	NP_775265.1:p.Val469Gly