Canonical Allele Identifier: CA2661538799

Gene: NR4A2

Linked Data

• gnomAD v4: 2-156325621-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325622dup , CM000664.2:g.156325622dup	GRCh38
NC_000002.11:g.157182134dup , CM000664.1:g.157182134dup	GRCh37
NC_000002.10:g.156890380dup	NCBI36
NG_011821.1:g.12154dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.*122dup	ENSP00000514865.1:n.*122dup
ENST00000700229.1:c.883dup
ENST00000700230.1:c.1459dup	ENSP00000514867.1:n.1459dup
ENST00000700231.1:c.*122dup	ENSP00000514868.1:n.*122dup
ENST00000339562.9:c.*122dup MANE Select	ENSP00000344479.4:n.*122dup
ENST00000675870.1:c.*430dup	ENSP00000502739.1:n.*430dup
ENST00000339562.8:c.*122dup	ENSP00000344479.4:n.*122dup
ENST00000409572.5:c.*122dup	ENSP00000386747.1:n.*122dup
ENST00000417764.5:c.*430dup	ENSP00000415632.1:n.*430dup
ENST00000417972.5:c.*430dup	ENSP00000394671.1:n.*430dup
ENST00000426264.5:c.*122dup	ENSP00000389986.1:n.*122dup
NM_006186.3:c.*122dup	NP_006177.1:n.*122dup
XM_005246621.2:c.*122dup	XP_005246678.1:n.*122dup
XM_005246622.2:c.*122dup	XP_005246679.1:n.*122dup
XM_005246623.1:c.*122dup	XP_005246680.1:n.*122dup
XM_006712553.2:c.*122dup	XP_006712616.1:n.*122dup
XM_011511246.1:c.*153dup	XP_011509548.1:n.*153dup
NM_173173.2:c.*122dup	NP_775265.1:n.*122dup
XM_005246621.4:c.*122dup	XP_005246678.1:n.*122dup
XM_006712553.4:c.*122dup	XP_006712616.1:n.*122dup
XM_011511246.2:c.*153dup	XP_011509548.1:n.*153dup
XM_017004219.2:c.*122dup	XP_016859708.1:n.*122dup
XM_017004220.2:c.*122dup	XP_016859709.1:n.*122dup
XR_001738751.2:n.2166dup
XR_001738752.2:n.1988dup
XR_427087.4:n.2045dup
NM_006186.4:c.*122dup MANE Select	NP_006177.1:n.*122dup
NM_173173.3:c.*122dup	NP_775265.1:n.*122dup