Canonical Allele Identifier: CA429727963

Gene: NR4A2

Linked Data

• MyVariant Identifiers: chr2:g.157186081G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156329569G>T , CM000664.2:g.156329569G>T	GRCh38
NC_000002.11:g.157186081G>T , CM000664.1:g.157186081G>T	GRCh37
NC_000002.10:g.156894327G>T	NCBI36
NG_011821.1:g.8207C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421709.2:c.429C>A	ENSP00000388120.2:p.Pro143=
ENST00000700228.1:c.489C>A	ENSP00000514865.1:p.Pro163=
ENST00000700230.1:c.51C>A	ENSP00000514867.1:p.Pro17=
ENST00000700231.1:c.618C>A	ENSP00000514868.1:p.Pro206=
ENST00000339562.9:c.618C>A MANE Select	ENSP00000344479.4:p.Pro206=
ENST00000675870.1:c.429C>A	ENSP00000502739.1:p.Pro143=
ENST00000339562.8:c.618C>A	ENSP00000344479.4:p.Pro206=
ENST00000406048.2:c.208+345C>A
ENST00000409108.6:c.618C>A	ENSP00000386993.2:p.Pro206=
ENST00000409572.5:c.618C>A	ENSP00000386747.1:p.Pro206=
ENST00000417764.5:c.429C>A	ENSP00000415632.1:p.Pro143=
ENST00000417972.5:c.429C>A	ENSP00000394671.1:p.Pro143=
ENST00000424077.1:c.618C>A	ENSP00000406808.1:p.Pro206=
ENST00000426264.5:c.429C>A	ENSP00000389986.1:p.Pro143=
ENST00000429376.5:c.429C>A	ENSP00000410952.1:p.Pro143=
NM_006186.3:c.618C>A	NP_006177.1:p.Pro206=
XM_005246621.2:c.651C>A	XP_005246678.1:p.Pro217=
XM_005246622.2:c.429C>A	XP_005246679.1:p.Pro143=
XM_005246623.1:c.429C>A	XP_005246680.1:p.Pro143=
XM_006712553.2:c.651C>A	XP_006712616.1:p.Pro217=
XM_011511246.1:c.651C>A	XP_011509548.1:p.Pro217=
XR_427087.2:n.2824C>A
NM_173173.2:c.429C>A	NP_775265.1:p.Pro143=
XM_005246621.4:c.651C>A	XP_005246678.1:p.Pro217=
XM_006712553.4:c.651C>A	XP_006712616.1:p.Pro217=
XM_011511246.2:c.651C>A	XP_011509548.1:p.Pro217=
XM_017004219.2:c.618C>A	XP_016859708.1:p.Pro206=
XM_017004220.2:c.618C>A	XP_016859709.1:p.Pro206=
XR_001738751.2:n.986C>A
XR_001738752.2:n.808C>A
XR_427087.4:n.865C>A
NM_006186.4:c.618C>A MANE Select	NP_006177.1:p.Pro206=
NM_173173.3:c.429C>A	NP_775265.1:p.Pro143=