Canonical Allele Identifier: CA348679554

Gene: NR4A2

Linked Data

• MyVariant Identifiers: chr2:g.157182381T>A (hg19) ; chr2:g.156325869T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325869T>A , CM000664.2:g.156325869T>A	GRCh38
NC_000002.11:g.157182381T>A , CM000664.1:g.157182381T>A	GRCh37
NC_000002.10:g.156890627T>A	NCBI36
NG_011821.1:g.11907A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1468A>T	ENSP00000514865.1:p.Lys490Ter
ENST00000700229.1:c.636A>T
ENST00000700230.1:c.1212A>T	ENSP00000514867.1:n.1212A>T
ENST00000700231.1:c.1597A>T	ENSP00000514868.1:p.Lys533Ter
ENST00000339562.9:c.1672A>T MANE Select	ENSP00000344479.4:p.Lys558Ter
ENST00000675870.1:c.*183A>T	ENSP00000502739.1:n.*183A>T
ENST00000339562.8:c.1672A>T	ENSP00000344479.4:p.Lys558Ter
ENST00000409108.6:c.1568A>T	ENSP00000386993.2:p.Glu523Val
ENST00000409572.5:c.1672A>T	ENSP00000386747.1:p.Lys558Ter
ENST00000417764.5:c.*183A>T	ENSP00000415632.1:n.*183A>T
ENST00000417972.5:c.*183A>T	ENSP00000394671.1:n.*183A>T
ENST00000426264.5:c.1483A>T	ENSP00000389986.1:p.Lys495Ter
ENST00000429376.5:c.1379A>T	ENSP00000410952.1:p.Glu460Val
NM_006186.3:c.1672A>T	NP_006177.1:p.Lys558Ter
XM_005246621.2:c.1705A>T	XP_005246678.1:p.Lys569Ter
XM_005246622.2:c.1483A>T	XP_005246679.1:p.Lys495Ter
XM_005246623.1:c.1483A>T	XP_005246680.1:p.Lys495Ter
XM_006712553.2:c.1630A>T	XP_006712616.1:p.Lys544Ter
XM_011511246.1:c.1601A>T	XP_011509548.1:p.Glu534Val
NM_173173.2:c.1483A>T	NP_775265.1:p.Lys495Ter
XM_005246621.4:c.1705A>T	XP_005246678.1:p.Lys569Ter
XM_006712553.4:c.1630A>T	XP_006712616.1:p.Lys544Ter
XM_011511246.2:c.1601A>T	XP_011509548.1:p.Glu534Val
XM_017004219.2:c.1672A>T	XP_016859708.1:p.Lys558Ter
XM_017004220.2:c.1597A>T	XP_016859709.1:p.Lys533Ter
XR_001738751.2:n.1919A>T
XR_001738752.2:n.1741A>T
XR_427087.4:n.1798A>T
NM_006186.4:c.1672A>T MANE Select	NP_006177.1:p.Lys558Ter
NM_173173.3:c.1483A>T	NP_775265.1:p.Lys495Ter