Canonical Allele Identifier: CA348681811

Gene: NR4A2

Linked Data

• COSMIC: COSM6207159 ; COSM6207160
• MyVariant Identifiers: chr2:g.157185971A>G (hg19) ; chr2:g.156329459A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156329459A>G , CM000664.2:g.156329459A>G	GRCh38
NC_000002.11:g.157185971A>G , CM000664.1:g.157185971A>G	GRCh37
NC_000002.10:g.156894217A>G	NCBI36
NG_011821.1:g.8317T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.599T>C	ENSP00000514865.1:p.Leu200Pro
ENST00000700230.1:c.161T>C	ENSP00000514867.1:p.Leu54Pro
ENST00000700231.1:c.728T>C	ENSP00000514868.1:p.Leu243Pro
ENST00000339562.9:c.728T>C MANE Select	ENSP00000344479.4:p.Leu243Pro
ENST00000675870.1:c.539T>C	ENSP00000502739.1:p.Leu180Pro
ENST00000339562.8:c.728T>C	ENSP00000344479.4:p.Leu243Pro
ENST00000406048.2:c.208+455T>C
ENST00000409108.6:c.728T>C	ENSP00000386993.2:p.Leu243Pro
ENST00000409572.5:c.728T>C	ENSP00000386747.1:p.Leu243Pro
ENST00000417764.5:c.539T>C	ENSP00000415632.1:p.Leu180Pro
ENST00000417972.5:c.539T>C	ENSP00000394671.1:p.Leu180Pro
ENST00000424077.1:c.728T>C	ENSP00000406808.1:p.Leu243Pro
ENST00000426264.5:c.539T>C	ENSP00000389986.1:p.Leu180Pro
ENST00000429376.5:c.539T>C	ENSP00000410952.1:p.Leu180Pro
NM_006186.3:c.728T>C	NP_006177.1:p.Leu243Pro
XM_005246621.2:c.761T>C	XP_005246678.1:p.Leu254Pro
XM_005246622.2:c.539T>C	XP_005246679.1:p.Leu180Pro
XM_005246623.1:c.539T>C	XP_005246680.1:p.Leu180Pro
XM_006712553.2:c.761T>C	XP_006712616.1:p.Leu254Pro
XM_011511246.1:c.761T>C	XP_011509548.1:p.Leu254Pro
XR_427087.2:n.2934T>C
NM_173173.2:c.539T>C	NP_775265.1:p.Leu180Pro
XM_005246621.4:c.761T>C	XP_005246678.1:p.Leu254Pro
XM_006712553.4:c.761T>C	XP_006712616.1:p.Leu254Pro
XM_011511246.2:c.761T>C	XP_011509548.1:p.Leu254Pro
XM_017004219.2:c.728T>C	XP_016859708.1:p.Leu243Pro
XM_017004220.2:c.728T>C	XP_016859709.1:p.Leu243Pro
XR_001738751.2:n.1096T>C
XR_001738752.2:n.918T>C
XR_427087.4:n.975T>C
NM_006186.4:c.728T>C MANE Select	NP_006177.1:p.Leu243Pro
NM_173173.3:c.539T>C	NP_775265.1:p.Leu180Pro