Canonical Allele Identifier: CA2739779155

Gene: NR4A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156332480T>A , CM000664.2:g.156332480T>A	GRCh38
NC_000002.11:g.157188992T>A , CM000664.1:g.157188992T>A	GRCh37
NC_000002.10:g.156897238T>A	NCBI36
NG_011821.1:g.5296A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421709.2:c.-14A>T	ENSP00000388120.2:n.-14A>T
ENST00000700228.1:c.-239A>T	ENSP00000514865.1:n.-239A>T
ENST00000700231.1:c.-127A>T	ENSP00000514868.1:n.-127A>T
ENST00000339562.9:c.-127A>T MANE Select	ENSP00000344479.4:n.-127A>T
ENST00000339562.8:c.-127A>T	ENSP00000344479.4:n.-127A>T
ENST00000409572.5:c.-126-1689A>T	ENSP00000386747.1:n.-126-1689A>T
ENST00000421709.1:c.-14A>T	ENSP00000388120.1:n.-14A>T
ENST00000424077.1:c.-3A>T	ENSP00000406808.1:n.-3A>T
ENST00000426264.5:c.-138A>T	ENSP00000389986.1:n.-138A>T
NM_006186.3:c.-127A>T	NP_006177.1:n.-127A>T
XM_005246621.2:c.31A>T	XP_005246678.1:p.Thr11Ser
XM_005246622.2:c.-138A>T	XP_005246679.1:n.-138A>T
XM_005246623.1:c.-14A>T	XP_005246680.1:n.-14A>T
XM_006712553.2:c.31A>T	XP_006712616.1:p.Thr11Ser
XM_011511246.1:c.31A>T	XP_011509548.1:p.Thr11Ser
XR_427087.2:n.2204A>T
NM_173173.2:c.-138A>T	NP_775265.1:n.-138A>T
XM_005246621.4:c.31A>T	XP_005246678.1:p.Thr11Ser
XM_006712553.4:c.31A>T	XP_006712616.1:p.Thr11Ser
XM_011511246.2:c.31A>T	XP_011509548.1:p.Thr11Ser
XM_017004220.2:c.-127A>T	XP_016859709.1:n.-127A>T
XR_001738751.2:n.242A>T
XR_001738752.2:n.242A>T
XR_427087.4:n.245A>T
NM_006186.4:c.-127A>T MANE Select	NP_006177.1:n.-127A>T
NM_173173.3:c.-138A>T	NP_775265.1:n.-138A>T