Canonical Allele Identifier: CA2661538814

Gene: NR4A2

Linked Data

• gnomAD v4: 2-156325644-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325644G>T , CM000664.2:g.156325644G>T	GRCh38
NC_000002.11:g.157182156G>T , CM000664.1:g.157182156G>T	GRCh37
NC_000002.10:g.156890402G>T	NCBI36
NG_011821.1:g.12132C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.*100C>A	ENSP00000514865.1:n.*100C>A
ENST00000700229.1:c.861C>A
ENST00000700230.1:c.1437C>A	ENSP00000514867.1:n.1437C>A
ENST00000700231.1:c.*100C>A	ENSP00000514868.1:n.*100C>A
ENST00000339562.9:c.*100C>A MANE Select	ENSP00000344479.4:n.*100C>A
ENST00000675870.1:c.*408C>A	ENSP00000502739.1:n.*408C>A
ENST00000339562.8:c.*100C>A	ENSP00000344479.4:n.*100C>A
ENST00000409572.5:c.*100C>A	ENSP00000386747.1:n.*100C>A
ENST00000417764.5:c.*408C>A	ENSP00000415632.1:n.*408C>A
ENST00000417972.5:c.*408C>A	ENSP00000394671.1:n.*408C>A
ENST00000426264.5:c.*100C>A	ENSP00000389986.1:n.*100C>A
NM_006186.3:c.*100C>A	NP_006177.1:n.*100C>A
XM_005246621.2:c.*100C>A	XP_005246678.1:n.*100C>A
XM_005246622.2:c.*100C>A	XP_005246679.1:n.*100C>A
XM_005246623.1:c.*100C>A	XP_005246680.1:n.*100C>A
XM_006712553.2:c.*100C>A	XP_006712616.1:n.*100C>A
XM_011511246.1:c.*131C>A	XP_011509548.1:n.*131C>A
NM_173173.2:c.*100C>A	NP_775265.1:n.*100C>A
XM_005246621.4:c.*100C>A	XP_005246678.1:n.*100C>A
XM_006712553.4:c.*100C>A	XP_006712616.1:n.*100C>A
XM_011511246.2:c.*131C>A	XP_011509548.1:n.*131C>A
XM_017004219.2:c.*100C>A	XP_016859708.1:n.*100C>A
XM_017004220.2:c.*100C>A	XP_016859709.1:n.*100C>A
XR_001738751.2:n.2144C>A
XR_001738752.2:n.1966C>A
XR_427087.4:n.2023C>A
NM_006186.4:c.*100C>A MANE Select	NP_006177.1:n.*100C>A
NM_173173.3:c.*100C>A	NP_775265.1:n.*100C>A