Canonical Allele Identifier: CA2661539676

Gene: NR4A2

Linked Data

• gnomAD v4: 2-156329546-T-TCCA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156329551_156329553dup , CM000664.2:g.156329551_156329553dup	GRCh38
NC_000002.11:g.157186063_157186065dup , CM000664.1:g.157186063_157186065dup	GRCh37
NC_000002.10:g.156894309_156894311dup	NCBI36
NG_011821.1:g.8227_8229dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421709.2:c.449_451dup	ENSP00000388120.2:p.Val150_Asp151insVal
ENST00000700228.1:c.509_511dup	ENSP00000514865.1:p.Val170_Asp171insVal
ENST00000700230.1:c.71_73dup	ENSP00000514867.1:p.Val24_Asp25insVal
ENST00000700231.1:c.638_640dup	ENSP00000514868.1:p.Val213_Asp214insVal
ENST00000339562.9:c.638_640dup MANE Select	ENSP00000344479.4:p.Val213_Asp214insVal
ENST00000675870.1:c.449_451dup	ENSP00000502739.1:p.Val150_Asp151insVal
ENST00000339562.8:c.638_640dup	ENSP00000344479.4:p.Val213_Asp214insVal
ENST00000406048.2:c.208+365_208+367dup
ENST00000409108.6:c.638_640dup	ENSP00000386993.2:p.Val213_Asp214insVal
ENST00000409572.5:c.638_640dup	ENSP00000386747.1:p.Val213_Asp214insVal
ENST00000417764.5:c.449_451dup	ENSP00000415632.1:p.Val150_Asp151insVal
ENST00000417972.5:c.449_451dup	ENSP00000394671.1:p.Val150_Asp151insVal
ENST00000424077.1:c.638_640dup	ENSP00000406808.1:p.Val213_Asp214insVal
ENST00000426264.5:c.449_451dup	ENSP00000389986.1:p.Val150_Asp151insVal
ENST00000429376.5:c.449_451dup	ENSP00000410952.1:p.Val150_Asp151insVal
NM_006186.3:c.638_640dup	NP_006177.1:p.Val213_Asp214insVal
XM_005246621.2:c.671_673dup	XP_005246678.1:p.Val224_Asp225insVal
XM_005246622.2:c.449_451dup	XP_005246679.1:p.Val150_Asp151insVal
XM_005246623.1:c.449_451dup	XP_005246680.1:p.Val150_Asp151insVal
XM_006712553.2:c.671_673dup	XP_006712616.1:p.Val224_Asp225insVal
XM_011511246.1:c.671_673dup	XP_011509548.1:p.Val224_Asp225insVal
XR_427087.2:n.2844_2846dup
NM_173173.2:c.449_451dup	NP_775265.1:p.Val150_Asp151insVal
XM_005246621.4:c.671_673dup	XP_005246678.1:p.Val224_Asp225insVal
XM_006712553.4:c.671_673dup	XP_006712616.1:p.Val224_Asp225insVal
XM_011511246.2:c.671_673dup	XP_011509548.1:p.Val224_Asp225insVal
XM_017004219.2:c.638_640dup	XP_016859708.1:p.Val213_Asp214insVal
XM_017004220.2:c.638_640dup	XP_016859709.1:p.Val213_Asp214insVal
XR_001738751.2:n.1006_1008dup
XR_001738752.2:n.828_830dup
XR_427087.4:n.885_887dup
NM_006186.4:c.638_640dup MANE Select	NP_006177.1:p.Val213_Asp214insVal
NM_173173.3:c.449_451dup	NP_775265.1:p.Val150_Asp151insVal