Canonical Allele Identifier: CA348679649

Gene: NR4A2

Linked Data

• MyVariant Identifiers: chr2:g.157182416A>G (hg19) ; chr2:g.156325904A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325904A>G , CM000664.2:g.156325904A>G	GRCh38
NC_000002.11:g.157182416A>G , CM000664.1:g.157182416A>G	GRCh37
NC_000002.10:g.156890662A>G	NCBI36
NG_011821.1:g.11872T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1433T>C	ENSP00000514865.1:p.Leu478Ser
ENST00000700229.1:c.601T>C
ENST00000700230.1:c.1177T>C	ENSP00000514867.1:n.1177T>C
ENST00000700231.1:c.1562T>C	ENSP00000514868.1:p.Leu521Ser
ENST00000339562.9:c.1637T>C MANE Select	ENSP00000344479.4:p.Leu546Ser
ENST00000675870.1:c.*148T>C	ENSP00000502739.1:n.*148T>C
ENST00000339562.8:c.1637T>C	ENSP00000344479.4:p.Leu546Ser
ENST00000409108.6:c.1533T>C	ENSP00000386993.2:p.Val511=
ENST00000409572.5:c.1637T>C	ENSP00000386747.1:p.Leu546Ser
ENST00000417764.5:c.*148T>C	ENSP00000415632.1:n.*148T>C
ENST00000417972.5:c.*148T>C	ENSP00000394671.1:n.*148T>C
ENST00000426264.5:c.1448T>C	ENSP00000389986.1:p.Leu483Ser
ENST00000429376.5:c.1344T>C	ENSP00000410952.1:p.Val448=
NM_006186.3:c.1637T>C	NP_006177.1:p.Leu546Ser
XM_005246621.2:c.1670T>C	XP_005246678.1:p.Leu557Ser
XM_005246622.2:c.1448T>C	XP_005246679.1:p.Leu483Ser
XM_005246623.1:c.1448T>C	XP_005246680.1:p.Leu483Ser
XM_006712553.2:c.1595T>C	XP_006712616.1:p.Leu532Ser
XM_011511246.1:c.1566T>C	XP_011509548.1:p.Val522=
NM_173173.2:c.1448T>C	NP_775265.1:p.Leu483Ser
XM_005246621.4:c.1670T>C	XP_005246678.1:p.Leu557Ser
XM_006712553.4:c.1595T>C	XP_006712616.1:p.Leu532Ser
XM_011511246.2:c.1566T>C	XP_011509548.1:p.Val522=
XM_017004219.2:c.1637T>C	XP_016859708.1:p.Leu546Ser
XM_017004220.2:c.1562T>C	XP_016859709.1:p.Leu521Ser
XR_001738751.2:n.1884T>C
XR_001738752.2:n.1706T>C
XR_427087.4:n.1763T>C
NM_006186.4:c.1637T>C MANE Select	NP_006177.1:p.Leu546Ser
NM_173173.3:c.1448T>C	NP_775265.1:p.Leu483Ser