Canonical Allele Identifier: CA348679548

Gene: NR4A2

Linked Data

• MyVariant Identifiers: chr2:g.157182379C>A (hg19) ; chr2:g.156325867C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325867C>A , CM000664.2:g.156325867C>A	GRCh38
NC_000002.11:g.157182379C>A , CM000664.1:g.157182379C>A	GRCh37
NC_000002.10:g.156890625C>A	NCBI36
NG_011821.1:g.11909G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1470G>T	ENSP00000514865.1:p.Lys490Asn
ENST00000700229.1:c.638G>T
ENST00000700230.1:c.1214G>T	ENSP00000514867.1:n.1214G>T
ENST00000700231.1:c.1599G>T	ENSP00000514868.1:p.Lys533Asn
ENST00000339562.9:c.1674G>T MANE Select	ENSP00000344479.4:p.Lys558Asn
ENST00000675870.1:c.*185G>T	ENSP00000502739.1:n.*185G>T
ENST00000339562.8:c.1674G>T	ENSP00000344479.4:p.Lys558Asn
ENST00000409108.6:c.1570G>T	ENSP00000386993.2:p.Ala524Ser
ENST00000409572.5:c.1674G>T	ENSP00000386747.1:p.Lys558Asn
ENST00000417764.5:c.*185G>T	ENSP00000415632.1:n.*185G>T
ENST00000417972.5:c.*185G>T	ENSP00000394671.1:n.*185G>T
ENST00000426264.5:c.1485G>T	ENSP00000389986.1:p.Lys495Asn
ENST00000429376.5:c.1381G>T	ENSP00000410952.1:p.Ala461Ser
NM_006186.3:c.1674G>T	NP_006177.1:p.Lys558Asn
XM_005246621.2:c.1707G>T	XP_005246678.1:p.Lys569Asn
XM_005246622.2:c.1485G>T	XP_005246679.1:p.Lys495Asn
XM_005246623.1:c.1485G>T	XP_005246680.1:p.Lys495Asn
XM_006712553.2:c.1632G>T	XP_006712616.1:p.Lys544Asn
XM_011511246.1:c.1603G>T	XP_011509548.1:p.Ala535Ser
NM_173173.2:c.1485G>T	NP_775265.1:p.Lys495Asn
XM_005246621.4:c.1707G>T	XP_005246678.1:p.Lys569Asn
XM_006712553.4:c.1632G>T	XP_006712616.1:p.Lys544Asn
XM_011511246.2:c.1603G>T	XP_011509548.1:p.Ala535Ser
XM_017004219.2:c.1674G>T	XP_016859708.1:p.Lys558Asn
XM_017004220.2:c.1599G>T	XP_016859709.1:p.Lys533Asn
XR_001738751.2:n.1921G>T
XR_001738752.2:n.1743G>T
XR_427087.4:n.1800G>T
NM_006186.4:c.1674G>T MANE Select	NP_006177.1:p.Lys558Asn
NM_173173.3:c.1485G>T	NP_775265.1:p.Lys495Asn