Canonical Allele Identifier: CA2521040030

Gene: NR4A2

Linked Data

• gnomAD v4: 2-156329796-TGGGCGTCGG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156329802_156329810del , CM000664.2:g.156329802_156329810del	GRCh38
NC_000002.11:g.157186314_157186322del , CM000664.1:g.157186314_157186322del	GRCh37
NC_000002.10:g.156894560_156894568del	NCBI36
NG_011821.1:g.7971_7979del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421709.2:c.193_201del	ENSP00000388120.2:p.Pro65_Pro67del
ENST00000700228.1:c.253_261del	ENSP00000514865.1:p.Pro85_Pro87del
ENST00000700231.1:c.382_390del	ENSP00000514868.1:p.Pro128_Pro130del
ENST00000339562.9:c.382_390del MANE Select	ENSP00000344479.4:p.Pro128_Pro130del
ENST00000675870.1:c.193_201del	ENSP00000502739.1:p.Pro65_Pro67del
ENST00000339562.8:c.382_390del	ENSP00000344479.4:p.Pro128_Pro130del
ENST00000406048.2:c.208+109_208+117del
ENST00000409108.6:c.382_390del	ENSP00000386993.2:p.Pro128_Pro130del
ENST00000409572.5:c.382_390del	ENSP00000386747.1:p.Pro128_Pro130del
ENST00000417764.5:c.193_201del	ENSP00000415632.1:p.Pro65_Pro67del
ENST00000417972.5:c.193_201del	ENSP00000394671.1:p.Pro65_Pro67del
ENST00000421709.1:c.193_201del	ENSP00000388120.1:p.Pro65_Pro67del
ENST00000424077.1:c.382_390del	ENSP00000406808.1:p.Pro128_Pro130del
ENST00000426264.5:c.193_201del	ENSP00000389986.1:p.Pro65_Pro67del
ENST00000429376.5:c.193_201del	ENSP00000410952.1:p.Pro65_Pro67del
NM_006186.3:c.382_390del	NP_006177.1:p.Pro128_Pro130del
XM_005246621.2:c.415_423del	XP_005246678.1:p.Pro139_Pro141del
XM_005246622.2:c.193_201del	XP_005246679.1:p.Pro65_Pro67del
XM_005246623.1:c.193_201del	XP_005246680.1:p.Pro65_Pro67del
XM_006712553.2:c.415_423del	XP_006712616.1:p.Pro139_Pro141del
XM_011511246.1:c.415_423del	XP_011509548.1:p.Pro139_Pro141del
XR_427087.2:n.2588_2596del
NM_173173.2:c.193_201del	NP_775265.1:p.Pro65_Pro67del
XM_005246621.4:c.415_423del	XP_005246678.1:p.Pro139_Pro141del
XM_006712553.4:c.415_423del	XP_006712616.1:p.Pro139_Pro141del
XM_011511246.2:c.415_423del	XP_011509548.1:p.Pro139_Pro141del
XM_017004219.2:c.382_390del	XP_016859708.1:p.Pro128_Pro130del
XM_017004220.2:c.382_390del	XP_016859709.1:p.Pro128_Pro130del
XR_001738751.2:n.750_758del
XR_001738752.2:n.572_580del
XR_427087.4:n.629_637del
NM_006186.4:c.382_390del MANE Select	NP_006177.1:p.Pro128_Pro130del
NM_173173.3:c.193_201del	NP_775265.1:p.Pro65_Pro67del