Canonical Allele Identifier: CA348679293

Gene: NR4A2

Linked Data

• COSMIC: COSM716255 ; COSM4859884
• MyVariant Identifiers: chr2:g.157182288C>G (hg19) ; chr2:g.156325776C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325776C>G , CM000664.2:g.156325776C>G	GRCh38
NC_000002.11:g.157182288C>G , CM000664.1:g.157182288C>G	GRCh37
NC_000002.10:g.156890534C>G	NCBI36
NG_011821.1:g.12000G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1561G>C	ENSP00000514865.1:p.Asp521His
ENST00000700229.1:c.729G>C
ENST00000700230.1:c.1305G>C	ENSP00000514867.1:n.1305G>C
ENST00000700231.1:c.1690G>C	ENSP00000514868.1:p.Asp564His
ENST00000339562.9:c.1765G>C MANE Select	ENSP00000344479.4:p.Asp589His
ENST00000675870.1:c.*276G>C	ENSP00000502739.1:n.*276G>C
ENST00000339562.8:c.1765G>C	ENSP00000344479.4:p.Asp589His
ENST00000409108.6:c.1661G>C	ENSP00000386993.2:p.Ter554Ser
ENST00000409572.5:c.1765G>C	ENSP00000386747.1:p.Asp589His
ENST00000417764.5:c.*276G>C	ENSP00000415632.1:n.*276G>C
ENST00000417972.5:c.*276G>C	ENSP00000394671.1:n.*276G>C
ENST00000426264.5:c.1576G>C	ENSP00000389986.1:p.Asp526His
ENST00000429376.5:c.1472G>C	ENSP00000410952.1:p.Ter491Ser
NM_006186.3:c.1765G>C	NP_006177.1:p.Asp589His
XM_005246621.2:c.1798G>C	XP_005246678.1:p.Asp600His
XM_005246622.2:c.1576G>C	XP_005246679.1:p.Asp526His
XM_005246623.1:c.1576G>C	XP_005246680.1:p.Asp526His
XM_006712553.2:c.1723G>C	XP_006712616.1:p.Asp575His
XM_011511246.1:c.1694G>C	XP_011509548.1:p.Ter565Ser
NM_173173.2:c.1576G>C	NP_775265.1:p.Asp526His
XM_005246621.4:c.1798G>C	XP_005246678.1:p.Asp600His
XM_006712553.4:c.1723G>C	XP_006712616.1:p.Asp575His
XM_011511246.2:c.1694G>C	XP_011509548.1:p.Ter565Ser
XM_017004219.2:c.1765G>C	XP_016859708.1:p.Asp589His
XM_017004220.2:c.1690G>C	XP_016859709.1:p.Asp564His
XR_001738751.2:n.2012G>C
XR_001738752.2:n.1834G>C
XR_427087.4:n.1891G>C
NM_006186.4:c.1765G>C MANE Select	NP_006177.1:p.Asp589His
NM_173173.3:c.1576G>C	NP_775265.1:p.Asp526His