Canonical Allele Identifier: CA1300460750

Gene: NR4A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156330210_156330212delinsAAC , CM000664.2:g.156330210_156330212delinsAAC	GRCh38
NC_000002.11:g.157186722_157186724delinsAAC , CM000664.1:g.157186722_157186724delinsAAC	GRCh37
NC_000002.10:g.156894968_156894970delinsAAC	NCBI36
NG_011821.1:g.7564_7566delinsGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421709.2:c.-13-202_-13-200delinsGTT	ENSP00000388120.2:n.-13-202_-13-200delinsGTT
ENST00000700228.1:c.-114-41_-114-39delinsGTT	ENSP00000514865.1:n.-114-41_-114-39delinsGTT
ENST00000700231.1:c.-2-24_-2-22delinsGTT	ENSP00000514868.1:n.-2-24_-2-22delinsGTT
ENST00000339562.9:c.-2-24_-2-22delinsGTT MANE Select	ENSP00000344479.4:n.-2-24_-2-22delinsGTT
ENST00000675870.1:c.-13-202_-13-200delinsGTT	ENSP00000502739.1:n.-13-202_-13-200delinsGTT
ENST00000339562.8:c.-2-24_-2-22delinsGTT	ENSP00000344479.4:n.-2-24_-2-22delinsGTT
ENST00000409108.6:c.-2-24_-2-22delinsGTT	ENSP00000386993.2:n.-2-24_-2-22delinsGTT
ENST00000409572.5:c.-2-24_-2-22delinsGTT	ENSP00000386747.1:n.-2-24_-2-22delinsGTT
ENST00000417764.5:c.-13-202_-13-200delinsGTT	ENSP00000415632.1:n.-13-202_-13-200delinsGTT
ENST00000417972.5:c.-13-202_-13-200delinsGTT	ENSP00000394671.1:n.-13-202_-13-200delinsGTT
ENST00000421709.1:c.-13-202_-13-200delinsGTT	ENSP00000388120.1:n.-13-202_-13-200delinsGTT
ENST00000424077.1:c.-2-24_-2-22delinsGTT	ENSP00000406808.1:n.-2-24_-2-22delinsGTT
ENST00000426264.5:c.-13-202_-13-200delinsGTT	ENSP00000389986.1:n.-13-202_-13-200delinsGTT
ENST00000429376.5:c.-13-202_-13-200delinsGTT	ENSP00000410952.1:n.-13-202_-13-200delinsGTT
NM_006186.3:c.-2-24_-2-22delinsGTT	NP_006177.1:n.-2-24_-2-22delinsGTT
XM_005246621.2:c.32-24_32-22delinsGTT	XP_005246678.1:n.32-24_32-22delinsGTT
XM_005246622.2:c.-13-202_-13-200delinsGTT	XP_005246679.1:n.-13-202_-13-200delinsGTT
XM_005246623.1:c.-13-202_-13-200delinsGTT	XP_005246680.1:n.-13-202_-13-200delinsGTT
XM_006712553.2:c.32-24_32-22delinsGTT	XP_006712616.1:n.32-24_32-22delinsGTT
XM_011511246.1:c.32-24_32-22delinsGTT	XP_011509548.1:n.32-24_32-22delinsGTT
XR_427087.2:n.2205-24_2205-22delinsGTT
NM_173173.2:c.-13-202_-13-200delinsGTT	NP_775265.1:n.-13-202_-13-200delinsGTT
XM_005246621.4:c.32-24_32-22delinsGTT	XP_005246678.1:n.32-24_32-22delinsGTT
XM_006712553.4:c.32-24_32-22delinsGTT	XP_006712616.1:n.32-24_32-22delinsGTT
XM_011511246.2:c.32-24_32-22delinsGTT	XP_011509548.1:n.32-24_32-22delinsGTT
XM_017004219.2:c.-2-24_-2-22delinsGTT	XP_016859708.1:n.-2-24_-2-22delinsGTT
XM_017004220.2:c.-2-24_-2-22delinsGTT	XP_016859709.1:n.-2-24_-2-22delinsGTT
XR_001738751.2:n.367-24_367-22delinsGTT
XR_001738752.2:n.367-202_367-200delinsGTT
XR_427087.4:n.246-24_246-22delinsGTT
NM_006186.4:c.-2-24_-2-22delinsGTT MANE Select	NP_006177.1:n.-2-24_-2-22delinsGTT
NM_173173.3:c.-13-202_-13-200delinsGTT	NP_775265.1:n.-13-202_-13-200delinsGTT