Canonical Allele Identifier: CA348682097

Gene: NR4A2

Linked Data

• MyVariant Identifiers: chr2:g.157186112C>G (hg19) ; chr2:g.156329600C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156329600C>G , CM000664.2:g.156329600C>G	GRCh38
NC_000002.11:g.157186112C>G , CM000664.1:g.157186112C>G	GRCh37
NC_000002.10:g.156894358C>G	NCBI36
NG_011821.1:g.8176G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421709.2:c.398G>C	ENSP00000388120.2:p.Gly133Ala
ENST00000700228.1:c.458G>C	ENSP00000514865.1:p.Gly153Ala
ENST00000700230.1:c.20G>C	ENSP00000514867.1:p.Gly7Ala
ENST00000700231.1:c.587G>C	ENSP00000514868.1:p.Gly196Ala
ENST00000339562.9:c.587G>C MANE Select	ENSP00000344479.4:p.Gly196Ala
ENST00000675870.1:c.398G>C	ENSP00000502739.1:p.Gly133Ala
ENST00000339562.8:c.587G>C	ENSP00000344479.4:p.Gly196Ala
ENST00000406048.2:c.208+314G>C
ENST00000409108.6:c.587G>C	ENSP00000386993.2:p.Gly196Ala
ENST00000409572.5:c.587G>C	ENSP00000386747.1:p.Gly196Ala
ENST00000417764.5:c.398G>C	ENSP00000415632.1:p.Gly133Ala
ENST00000417972.5:c.398G>C	ENSP00000394671.1:p.Gly133Ala
ENST00000424077.1:c.587G>C	ENSP00000406808.1:p.Gly196Ala
ENST00000426264.5:c.398G>C	ENSP00000389986.1:p.Gly133Ala
ENST00000429376.5:c.398G>C	ENSP00000410952.1:p.Gly133Ala
NM_006186.3:c.587G>C	NP_006177.1:p.Gly196Ala
XM_005246621.2:c.620G>C	XP_005246678.1:p.Gly207Ala
XM_005246622.2:c.398G>C	XP_005246679.1:p.Gly133Ala
XM_005246623.1:c.398G>C	XP_005246680.1:p.Gly133Ala
XM_006712553.2:c.620G>C	XP_006712616.1:p.Gly207Ala
XM_011511246.1:c.620G>C	XP_011509548.1:p.Gly207Ala
XR_427087.2:n.2793G>C
NM_173173.2:c.398G>C	NP_775265.1:p.Gly133Ala
XM_005246621.4:c.620G>C	XP_005246678.1:p.Gly207Ala
XM_006712553.4:c.620G>C	XP_006712616.1:p.Gly207Ala
XM_011511246.2:c.620G>C	XP_011509548.1:p.Gly207Ala
XM_017004219.2:c.587G>C	XP_016859708.1:p.Gly196Ala
XM_017004220.2:c.587G>C	XP_016859709.1:p.Gly196Ala
XR_001738751.2:n.955G>C
XR_001738752.2:n.777G>C
XR_427087.4:n.834G>C
NM_006186.4:c.587G>C MANE Select	NP_006177.1:p.Gly196Ala
NM_173173.3:c.398G>C	NP_775265.1:p.Gly133Ala