Canonical Allele Identifier: CA429728052

Gene: NR4A2

Linked Data

• COSMIC: COSM4085777 ; COSM4906967
• MyVariant Identifiers: chr2:g.157186467A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156329955A>G , CM000664.2:g.156329955A>G	GRCh38
NC_000002.11:g.157186467A>G , CM000664.1:g.157186467A>G	GRCh37
NC_000002.10:g.156894713A>G	NCBI36
NG_011821.1:g.7821T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421709.2:c.43T>C	ENSP00000388120.2:p.Leu15=
ENST00000700228.1:c.103T>C	ENSP00000514865.1:p.Leu35=
ENST00000700231.1:c.232T>C	ENSP00000514868.1:p.Leu78=
ENST00000339562.9:c.232T>C MANE Select	ENSP00000344479.4:p.Leu78=
ENST00000675870.1:c.43T>C	ENSP00000502739.1:p.Leu15=
ENST00000339562.8:c.232T>C	ENSP00000344479.4:p.Leu78=
ENST00000406048.2:c.167T>C
ENST00000409108.6:c.232T>C	ENSP00000386993.2:p.Leu78=
ENST00000409572.5:c.232T>C	ENSP00000386747.1:p.Leu78=
ENST00000417764.5:c.43T>C	ENSP00000415632.1:p.Leu15=
ENST00000417972.5:c.43T>C	ENSP00000394671.1:p.Leu15=
ENST00000421709.1:c.43T>C	ENSP00000388120.1:p.Leu15=
ENST00000424077.1:c.232T>C	ENSP00000406808.1:p.Leu78=
ENST00000426264.5:c.43T>C	ENSP00000389986.1:p.Leu15=
ENST00000429376.5:c.43T>C	ENSP00000410952.1:p.Leu15=
NM_006186.3:c.232T>C	NP_006177.1:p.Leu78=
XM_005246621.2:c.265T>C	XP_005246678.1:p.Leu89=
XM_005246622.2:c.43T>C	XP_005246679.1:p.Leu15=
XM_005246623.1:c.43T>C	XP_005246680.1:p.Leu15=
XM_006712553.2:c.265T>C	XP_006712616.1:p.Leu89=
XM_011511246.1:c.265T>C	XP_011509548.1:p.Leu89=
XR_427087.2:n.2438T>C
NM_173173.2:c.43T>C	NP_775265.1:p.Leu15=
XM_005246621.4:c.265T>C	XP_005246678.1:p.Leu89=
XM_006712553.4:c.265T>C	XP_006712616.1:p.Leu89=
XM_011511246.2:c.265T>C	XP_011509548.1:p.Leu89=
XM_017004219.2:c.232T>C	XP_016859708.1:p.Leu78=
XM_017004220.2:c.232T>C	XP_016859709.1:p.Leu78=
XR_001738751.2:n.600T>C
XR_001738752.2:n.422T>C
XR_427087.4:n.479T>C
NM_006186.4:c.232T>C MANE Select	NP_006177.1:p.Leu78=
NM_173173.3:c.43T>C	NP_775265.1:p.Leu15=