Canonical Allele Identifier: CA913089311

Gene: NR4A2

Linked Data

• ClinVar Variation Id: 996680
• ClinVar RCV Id: RCV001291378
• dbSNP Id: rs1686821540
• MyVariant Identifiers: chr2:g.157186097_157186098insGGAC (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156329587_156329590dup , CM000664.2:g.156329587_156329590dup	GRCh38
NC_000002.11:g.157186099_157186102dup , CM000664.1:g.157186099_157186102dup	GRCh37
NC_000002.10:g.156894345_156894348dup	NCBI36
NG_011821.1:g.8187_8190dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421709.2:c.409_412dup	ENSP00000388120.2:p.Pro138ArgfsTer?
ENST00000700228.1:c.469_472dup	ENSP00000514865.1:p.Pro158ArgfsTer?
ENST00000700230.1:c.31_34dup	ENSP00000514867.1:p.Pro12ArgfsTer?
ENST00000700231.1:c.598_601dup	ENSP00000514868.1:p.Pro201ArgfsTer?
ENST00000339562.9:c.598_601dup MANE Select	ENSP00000344479.4:p.Pro201ArgfsTer?
ENST00000675870.1:c.409_412dup	ENSP00000502739.1:p.Pro138ArgfsTer?
ENST00000339562.8:c.598_601dup	ENSP00000344479.4:p.Pro201ArgfsTer?
ENST00000406048.2:c.208+325_208+328dup
ENST00000409108.6:c.598_601dup	ENSP00000386993.2:p.Pro201ArgfsTer?
ENST00000409572.5:c.598_601dup	ENSP00000386747.1:p.Pro201ArgfsTer?
ENST00000417764.5:c.409_412dup	ENSP00000415632.1:p.Pro138ArgfsTer?
ENST00000417972.5:c.409_412dup	ENSP00000394671.1:p.Pro138ArgfsTer?
ENST00000424077.1:c.598_601dup	ENSP00000406808.1:p.Pro201ArgfsTer?
ENST00000426264.5:c.409_412dup	ENSP00000389986.1:p.Pro138ArgfsTer?
ENST00000429376.5:c.409_412dup	ENSP00000410952.1:p.Pro138ArgfsTer?
NM_006186.3:c.598_601dup	NP_006177.1:p.Pro201ArgfsTer?
XM_005246621.2:c.631_634dup	XP_005246678.1:p.Pro212ArgfsTer?
XM_005246622.2:c.409_412dup	XP_005246679.1:p.Pro138ArgfsTer?
XM_005246623.1:c.409_412dup	XP_005246680.1:p.Pro138ArgfsTer?
XM_006712553.2:c.631_634dup	XP_006712616.1:p.Pro212ArgfsTer?
XM_011511246.1:c.631_634dup	XP_011509548.1:p.Pro212ArgfsTer?
XR_427087.2:n.2804_2807dup
NM_173173.2:c.409_412dup	NP_775265.1:p.Pro138ArgfsTer?
XM_005246621.4:c.631_634dup	XP_005246678.1:p.Pro212ArgfsTer?
XM_006712553.4:c.631_634dup	XP_006712616.1:p.Pro212ArgfsTer?
XM_011511246.2:c.631_634dup	XP_011509548.1:p.Pro212ArgfsTer?
XM_017004219.2:c.598_601dup	XP_016859708.1:p.Pro201ArgfsTer?
XM_017004220.2:c.598_601dup	XP_016859709.1:p.Pro201ArgfsTer?
XR_001738751.2:n.966_969dup
XR_001738752.2:n.788_791dup
XR_427087.4:n.845_848dup
NM_006186.4:c.598_601dup MANE Select	NP_006177.1:p.Pro201ArgfsTer?
NM_173173.3:c.409_412dup	NP_775265.1:p.Pro138ArgfsTer?