Canonical Allele Identifier: CA348679829

Gene: NR4A2

Linked Data

• MyVariant Identifiers: chr2:g.157182482A>C (hg19) ; chr2:g.156325970A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325970A>C , CM000664.2:g.156325970A>C	GRCh38
NC_000002.11:g.157182482A>C , CM000664.1:g.157182482A>C	GRCh37
NC_000002.10:g.156890728A>C	NCBI36
NG_011821.1:g.11806T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1367T>G	ENSP00000514865.1:p.Val456Gly
ENST00000700229.1:c.535T>G
ENST00000700230.1:c.1111T>G	ENSP00000514867.1:n.1111T>G
ENST00000700231.1:c.1496T>G	ENSP00000514868.1:p.Val499Gly
ENST00000339562.9:c.1571T>G MANE Select	ENSP00000344479.4:p.Val524Gly
ENST00000675870.1:c.*82T>G	ENSP00000502739.1:n.*82T>G
ENST00000339562.8:c.1571T>G	ENSP00000344479.4:p.Val524Gly
ENST00000409108.6:c.1467T>G	ENSP00000386993.2:p.Ser489Arg
ENST00000409572.5:c.1571T>G	ENSP00000386747.1:p.Val524Gly
ENST00000417764.5:c.*82T>G	ENSP00000415632.1:n.*82T>G
ENST00000417972.5:c.*82T>G	ENSP00000394671.1:n.*82T>G
ENST00000426264.5:c.1382T>G	ENSP00000389986.1:p.Val461Gly
ENST00000429376.5:c.1278T>G	ENSP00000410952.1:p.Ser426Arg
NM_006186.3:c.1571T>G	NP_006177.1:p.Val524Gly
XM_005246621.2:c.1604T>G	XP_005246678.1:p.Val535Gly
XM_005246622.2:c.1382T>G	XP_005246679.1:p.Val461Gly
XM_005246623.1:c.1382T>G	XP_005246680.1:p.Val461Gly
XM_006712553.2:c.1529T>G	XP_006712616.1:p.Val510Gly
XM_011511246.1:c.1500T>G	XP_011509548.1:p.Ser500Arg
XR_427087.2:n.3656T>G
NM_173173.2:c.1382T>G	NP_775265.1:p.Val461Gly
XM_005246621.4:c.1604T>G	XP_005246678.1:p.Val535Gly
XM_006712553.4:c.1529T>G	XP_006712616.1:p.Val510Gly
XM_011511246.2:c.1500T>G	XP_011509548.1:p.Ser500Arg
XM_017004219.2:c.1571T>G	XP_016859708.1:p.Val524Gly
XM_017004220.2:c.1496T>G	XP_016859709.1:p.Val499Gly
XR_001738751.2:n.1818T>G
XR_001738752.2:n.1640T>G
XR_427087.4:n.1697T>G
NM_006186.4:c.1571T>G MANE Select	NP_006177.1:p.Val524Gly
NM_173173.3:c.1382T>G	NP_775265.1:p.Val461Gly