Canonical Allele Identifier: CA1300460748

Gene: NR4A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156330209_156330210delinsTA , CM000664.2:g.156330209_156330210delinsTA	GRCh38
NC_000002.11:g.157186721_157186722delinsTA , CM000664.1:g.157186721_157186722delinsTA	GRCh37
NC_000002.10:g.156894967_156894968delinsTA	NCBI36
NG_011821.1:g.7566_7567delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421709.2:c.-13-200_-13-199delinsTA	ENSP00000388120.2:n.-13-200_-13-199delinsTA
ENST00000700228.1:c.-114-39_-114-38delinsTA	ENSP00000514865.1:n.-114-39_-114-38delinsTA
ENST00000700231.1:c.-2-22_-2-21delinsTA	ENSP00000514868.1:n.-2-22_-2-21delinsTA
ENST00000339562.9:c.-2-22_-2-21delinsTA MANE Select	ENSP00000344479.4:n.-2-22_-2-21delinsTA
ENST00000675870.1:c.-13-200_-13-199delinsTA	ENSP00000502739.1:n.-13-200_-13-199delinsTA
ENST00000339562.8:c.-2-22_-2-21delinsTA	ENSP00000344479.4:n.-2-22_-2-21delinsTA
ENST00000409108.6:c.-2-22_-2-21delinsTA	ENSP00000386993.2:n.-2-22_-2-21delinsTA
ENST00000409572.5:c.-2-22_-2-21delinsTA	ENSP00000386747.1:n.-2-22_-2-21delinsTA
ENST00000417764.5:c.-13-200_-13-199delinsTA	ENSP00000415632.1:n.-13-200_-13-199delinsTA
ENST00000417972.5:c.-13-200_-13-199delinsTA	ENSP00000394671.1:n.-13-200_-13-199delinsTA
ENST00000421709.1:c.-13-200_-13-199delinsTA	ENSP00000388120.1:n.-13-200_-13-199delinsTA
ENST00000424077.1:c.-2-22_-2-21delinsTA	ENSP00000406808.1:n.-2-22_-2-21delinsTA
ENST00000426264.5:c.-13-200_-13-199delinsTA	ENSP00000389986.1:n.-13-200_-13-199delinsTA
ENST00000429376.5:c.-13-200_-13-199delinsTA	ENSP00000410952.1:n.-13-200_-13-199delinsTA
NM_006186.3:c.-2-22_-2-21delinsTA	NP_006177.1:n.-2-22_-2-21delinsTA
XM_005246621.2:c.32-22_32-21delinsTA	XP_005246678.1:n.32-22_32-21delinsTA
XM_005246622.2:c.-13-200_-13-199delinsTA	XP_005246679.1:n.-13-200_-13-199delinsTA
XM_005246623.1:c.-13-200_-13-199delinsTA	XP_005246680.1:n.-13-200_-13-199delinsTA
XM_006712553.2:c.32-22_32-21delinsTA	XP_006712616.1:n.32-22_32-21delinsTA
XM_011511246.1:c.32-22_32-21delinsTA	XP_011509548.1:n.32-22_32-21delinsTA
XR_427087.2:n.2205-22_2205-21delinsTA
NM_173173.2:c.-13-200_-13-199delinsTA	NP_775265.1:n.-13-200_-13-199delinsTA
XM_005246621.4:c.32-22_32-21delinsTA	XP_005246678.1:n.32-22_32-21delinsTA
XM_006712553.4:c.32-22_32-21delinsTA	XP_006712616.1:n.32-22_32-21delinsTA
XM_011511246.2:c.32-22_32-21delinsTA	XP_011509548.1:n.32-22_32-21delinsTA
XM_017004219.2:c.-2-22_-2-21delinsTA	XP_016859708.1:n.-2-22_-2-21delinsTA
XM_017004220.2:c.-2-22_-2-21delinsTA	XP_016859709.1:n.-2-22_-2-21delinsTA
XR_001738751.2:n.367-22_367-21delinsTA
XR_001738752.2:n.367-200_367-199delinsTA
XR_427087.4:n.246-22_246-21delinsTA
NM_006186.4:c.-2-22_-2-21delinsTA MANE Select	NP_006177.1:n.-2-22_-2-21delinsTA
NM_173173.3:c.-13-200_-13-199delinsTA	NP_775265.1:n.-13-200_-13-199delinsTA