Canonical Allele Identifier: CA15148874

Gene: NR4A2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156331633C>T , CM000664.2:g.156331633C>T	GRCh38
NC_000002.11:g.157188145C>T , CM000664.1:g.157188145C>T	GRCh37
NC_000002.10:g.156896391C>T	NCBI36
NG_011821.1:g.6143G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421709.2:c.-14+847G>A	ENSP00000388120.2:n.-14+847G>A
ENST00000700228.1:c.-238-842G>A	ENSP00000514865.1:n.-238-842G>A
ENST00000700231.1:c.-126-842G>A	ENSP00000514868.1:n.-126-842G>A
ENST00000339562.9:c.-126-842G>A MANE Select	ENSP00000344479.4:n.-126-842G>A
ENST00000339562.8:c.-126-842G>A	ENSP00000344479.4:n.-126-842G>A
ENST00000409572.5:c.-126-842G>A	ENSP00000386747.1:n.-126-842G>A
ENST00000417972.5:c.-138+151G>A	ENSP00000394671.1:n.-138+151G>A
ENST00000421709.1:c.-14+847G>A	ENSP00000388120.1:n.-14+847G>A
ENST00000424077.1:c.-3+847G>A	ENSP00000406808.1:n.-3+847G>A
ENST00000426264.5:c.-137-842G>A	ENSP00000389986.1:n.-137-842G>A
NM_006186.3:c.-126-842G>A	NP_006177.1:n.-126-842G>A
XM_005246621.2:c.31+847G>A	XP_005246678.1:n.31+847G>A
XM_005246622.2:c.-137-842G>A	XP_005246679.1:n.-137-842G>A
XM_005246623.1:c.-14+847G>A	XP_005246680.1:n.-14+847G>A
XM_006712553.2:c.31+847G>A	XP_006712616.1:n.31+847G>A
XM_011511246.1:c.31+847G>A	XP_011509548.1:n.31+847G>A
XR_427087.2:n.2204+847G>A
NM_173173.2:c.-137-842G>A	NP_775265.1:n.-137-842G>A
XM_005246621.4:c.31+847G>A	XP_005246678.1:n.31+847G>A
XM_006712553.4:c.31+847G>A	XP_006712616.1:n.31+847G>A
XM_011511246.2:c.31+847G>A	XP_011509548.1:n.31+847G>A
XM_017004220.2:c.-126-842G>A	XP_016859709.1:n.-126-842G>A
XR_001738751.2:n.243-842G>A
XR_001738752.2:n.243-842G>A
XR_427087.4:n.245+847G>A
NM_006186.4:c.-126-842G>A MANE Select	NP_006177.1:n.-126-842G>A
NM_173173.3:c.-137-842G>A	NP_775265.1:n.-137-842G>A