Canonical Allele Identifier: CA348679384

Gene: NR4A2

Linked Data

• MyVariant Identifiers: chr2:g.157182320A>G (hg19) ; chr2:g.156325808A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325808A>G , CM000664.2:g.156325808A>G	GRCh38
NC_000002.11:g.157182320A>G , CM000664.1:g.157182320A>G	GRCh37
NC_000002.10:g.156890566A>G	NCBI36
NG_011821.1:g.11968T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1529T>C	ENSP00000514865.1:p.Leu510Ser
ENST00000700229.1:c.697T>C
ENST00000700230.1:c.1273T>C	ENSP00000514867.1:n.1273T>C
ENST00000700231.1:c.1658T>C	ENSP00000514868.1:p.Leu553Ser
ENST00000339562.9:c.1733T>C MANE Select	ENSP00000344479.4:p.Leu578Ser
ENST00000675870.1:c.*244T>C	ENSP00000502739.1:n.*244T>C
ENST00000339562.8:c.1733T>C	ENSP00000344479.4:p.Leu578Ser
ENST00000409108.6:c.1629T>C	ENSP00000386993.2:p.Ile543=
ENST00000409572.5:c.1733T>C	ENSP00000386747.1:p.Leu578Ser
ENST00000417764.5:c.*244T>C	ENSP00000415632.1:n.*244T>C
ENST00000417972.5:c.*244T>C	ENSP00000394671.1:n.*244T>C
ENST00000426264.5:c.1544T>C	ENSP00000389986.1:p.Leu515Ser
ENST00000429376.5:c.1440T>C	ENSP00000410952.1:p.Ile480=
NM_006186.3:c.1733T>C	NP_006177.1:p.Leu578Ser
XM_005246621.2:c.1766T>C	XP_005246678.1:p.Leu589Ser
XM_005246622.2:c.1544T>C	XP_005246679.1:p.Leu515Ser
XM_005246623.1:c.1544T>C	XP_005246680.1:p.Leu515Ser
XM_006712553.2:c.1691T>C	XP_006712616.1:p.Leu564Ser
XM_011511246.1:c.1662T>C	XP_011509548.1:p.Ile554=
NM_173173.2:c.1544T>C	NP_775265.1:p.Leu515Ser
XM_005246621.4:c.1766T>C	XP_005246678.1:p.Leu589Ser
XM_006712553.4:c.1691T>C	XP_006712616.1:p.Leu564Ser
XM_011511246.2:c.1662T>C	XP_011509548.1:p.Ile554=
XM_017004219.2:c.1733T>C	XP_016859708.1:p.Leu578Ser
XM_017004220.2:c.1658T>C	XP_016859709.1:p.Leu553Ser
XR_001738751.2:n.1980T>C
XR_001738752.2:n.1802T>C
XR_427087.4:n.1859T>C
NM_006186.4:c.1733T>C MANE Select	NP_006177.1:p.Leu578Ser
NM_173173.3:c.1544T>C	NP_775265.1:p.Leu515Ser