Canonical Allele Identifier: CA2842004113

Gene: NR4A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156329642_156329643del , CM000664.2:g.156329642_156329643del	GRCh38
NC_000002.11:g.157186154_157186155del , CM000664.1:g.157186154_157186155del	GRCh37
NC_000002.10:g.156894400_156894401del	NCBI36
NG_011821.1:g.8136_8137del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421709.2:c.358_359del	ENSP00000388120.2:p.Pro120TrpfsTer6
ENST00000700228.1:c.418_419del	ENSP00000514865.1:p.Pro140TrpfsTer6
ENST00000700231.1:c.547_548del	ENSP00000514868.1:p.Pro183TrpfsTer6
ENST00000339562.9:c.547_548del MANE Select	ENSP00000344479.4:p.Pro183TrpfsTer6
ENST00000675870.1:c.358_359del	ENSP00000502739.1:p.Pro120TrpfsTer6
ENST00000339562.8:c.547_548del	ENSP00000344479.4:p.Pro183TrpfsTer6
ENST00000406048.2:c.208+274_208+275del
ENST00000409108.6:c.547_548del	ENSP00000386993.2:p.Pro183TrpfsTer6
ENST00000409572.5:c.547_548del	ENSP00000386747.1:p.Pro183TrpfsTer6
ENST00000417764.5:c.358_359del	ENSP00000415632.1:p.Pro120TrpfsTer6
ENST00000417972.5:c.358_359del	ENSP00000394671.1:p.Pro120TrpfsTer6
ENST00000424077.1:c.547_548del	ENSP00000406808.1:p.Pro183TrpfsTer6
ENST00000426264.5:c.358_359del	ENSP00000389986.1:p.Pro120TrpfsTer6
ENST00000429376.5:c.358_359del	ENSP00000410952.1:p.Pro120TrpfsTer6
NM_006186.3:c.547_548del	NP_006177.1:p.Pro183TrpfsTer6
XM_005246621.2:c.580_581del	XP_005246678.1:p.Pro194TrpfsTer6
XM_005246622.2:c.358_359del	XP_005246679.1:p.Pro120TrpfsTer6
XM_005246623.1:c.358_359del	XP_005246680.1:p.Pro120TrpfsTer6
XM_006712553.2:c.580_581del	XP_006712616.1:p.Pro194TrpfsTer6
XM_011511246.1:c.580_581del	XP_011509548.1:p.Pro194TrpfsTer6
XR_427087.2:n.2753_2754del
NM_173173.2:c.358_359del	NP_775265.1:p.Pro120TrpfsTer6
XM_005246621.4:c.580_581del	XP_005246678.1:p.Pro194TrpfsTer6
XM_006712553.4:c.580_581del	XP_006712616.1:p.Pro194TrpfsTer6
XM_011511246.2:c.580_581del	XP_011509548.1:p.Pro194TrpfsTer6
XM_017004219.2:c.547_548del	XP_016859708.1:p.Pro183TrpfsTer6
XM_017004220.2:c.547_548del	XP_016859709.1:p.Pro183TrpfsTer6
XR_001738751.2:n.915_916del
XR_001738752.2:n.737_738del
XR_427087.4:n.794_795del
NM_006186.4:c.547_548del MANE Select	NP_006177.1:p.Pro183TrpfsTer6
NM_173173.3:c.358_359del	NP_775265.1:p.Pro120TrpfsTer6