Canonical Allele Identifier: CA348679891

Gene: NR4A2

Linked Data

• MyVariant Identifiers: chr2:g.157182504C>A (hg19) ; chr2:g.156325992C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325992C>A , CM000664.2:g.156325992C>A	GRCh38
NC_000002.11:g.157182504C>A , CM000664.1:g.157182504C>A	GRCh37
NC_000002.10:g.156890750C>A	NCBI36
NG_011821.1:g.11784G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1345G>T	ENSP00000514865.1:p.Gly449Trp
ENST00000700229.1:c.513G>T
ENST00000700230.1:c.1089G>T	ENSP00000514867.1:n.1089G>T
ENST00000700231.1:c.1474G>T	ENSP00000514868.1:p.Gly492Trp
ENST00000339562.9:c.1549G>T MANE Select	ENSP00000344479.4:p.Gly517Trp
ENST00000675870.1:c.*60G>T	ENSP00000502739.1:n.*60G>T
ENST00000339562.8:c.1549G>T	ENSP00000344479.4:p.Gly517Trp
ENST00000409108.6:c.1445G>T	ENSP00000386993.2:p.Arg482Leu
ENST00000409572.5:c.1549G>T	ENSP00000386747.1:p.Gly517Trp
ENST00000417764.5:c.*60G>T	ENSP00000415632.1:n.*60G>T
ENST00000417972.5:c.*60G>T	ENSP00000394671.1:n.*60G>T
ENST00000426264.5:c.1360G>T	ENSP00000389986.1:p.Gly454Trp
ENST00000429376.5:c.1256G>T	ENSP00000410952.1:p.Arg419Leu
NM_006186.3:c.1549G>T	NP_006177.1:p.Gly517Trp
XM_005246621.2:c.1582G>T	XP_005246678.1:p.Gly528Trp
XM_005246622.2:c.1360G>T	XP_005246679.1:p.Gly454Trp
XM_005246623.1:c.1360G>T	XP_005246680.1:p.Gly454Trp
XM_006712553.2:c.1507G>T	XP_006712616.1:p.Gly503Trp
XM_011511246.1:c.1478G>T	XP_011509548.1:p.Arg493Leu
XR_427087.2:n.3634G>T
NM_173173.2:c.1360G>T	NP_775265.1:p.Gly454Trp
XM_005246621.4:c.1582G>T	XP_005246678.1:p.Gly528Trp
XM_006712553.4:c.1507G>T	XP_006712616.1:p.Gly503Trp
XM_011511246.2:c.1478G>T	XP_011509548.1:p.Arg493Leu
XM_017004219.2:c.1549G>T	XP_016859708.1:p.Gly517Trp
XM_017004220.2:c.1474G>T	XP_016859709.1:p.Gly492Trp
XR_001738751.2:n.1796G>T
XR_001738752.2:n.1618G>T
XR_427087.4:n.1675G>T
NM_006186.4:c.1549G>T MANE Select	NP_006177.1:p.Gly517Trp
NM_173173.3:c.1360G>T	NP_775265.1:p.Gly454Trp