Canonical Allele Identifier: CA348679702

Gene: NR4A2

Linked Data

• MyVariant Identifiers: chr2:g.157182437A>G (hg19) ; chr2:g.156325925A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325925A>G , CM000664.2:g.156325925A>G	GRCh38
NC_000002.11:g.157182437A>G , CM000664.1:g.157182437A>G	GRCh37
NC_000002.10:g.156890683A>G	NCBI36
NG_011821.1:g.11851T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1412T>C	ENSP00000514865.1:p.Val471Ala
ENST00000700229.1:c.580T>C
ENST00000700230.1:c.1156T>C	ENSP00000514867.1:n.1156T>C
ENST00000700231.1:c.1541T>C	ENSP00000514868.1:p.Val514Ala
ENST00000339562.9:c.1616T>C MANE Select	ENSP00000344479.4:p.Val539Ala
ENST00000675870.1:c.*127T>C	ENSP00000502739.1:n.*127T>C
ENST00000339562.8:c.1616T>C	ENSP00000344479.4:p.Val539Ala
ENST00000409108.6:c.1512T>C	ENSP00000386993.2:p.Arg504=
ENST00000409572.5:c.1616T>C	ENSP00000386747.1:p.Val539Ala
ENST00000417764.5:c.*127T>C	ENSP00000415632.1:n.*127T>C
ENST00000417972.5:c.*127T>C	ENSP00000394671.1:n.*127T>C
ENST00000426264.5:c.1427T>C	ENSP00000389986.1:p.Val476Ala
ENST00000429376.5:c.1323T>C	ENSP00000410952.1:p.Arg441=
NM_006186.3:c.1616T>C	NP_006177.1:p.Val539Ala
XM_005246621.2:c.1649T>C	XP_005246678.1:p.Val550Ala
XM_005246622.2:c.1427T>C	XP_005246679.1:p.Val476Ala
XM_005246623.1:c.1427T>C	XP_005246680.1:p.Val476Ala
XM_006712553.2:c.1574T>C	XP_006712616.1:p.Val525Ala
XM_011511246.1:c.1545T>C	XP_011509548.1:p.Arg515=
NM_173173.2:c.1427T>C	NP_775265.1:p.Val476Ala
XM_005246621.4:c.1649T>C	XP_005246678.1:p.Val550Ala
XM_006712553.4:c.1574T>C	XP_006712616.1:p.Val525Ala
XM_011511246.2:c.1545T>C	XP_011509548.1:p.Arg515=
XM_017004219.2:c.1616T>C	XP_016859708.1:p.Val539Ala
XM_017004220.2:c.1541T>C	XP_016859709.1:p.Val514Ala
XR_001738751.2:n.1863T>C
XR_001738752.2:n.1685T>C
XR_427087.4:n.1742T>C
NM_006186.4:c.1616T>C MANE Select	NP_006177.1:p.Val539Ala
NM_173173.3:c.1427T>C	NP_775265.1:p.Val476Ala