Canonical Allele Identifier: CA348679582

Gene: NR4A2

Linked Data

• MyVariant Identifiers: chr2:g.157182390G>T (hg19) ; chr2:g.156325878G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325878G>T , CM000664.2:g.156325878G>T	GRCh38
NC_000002.11:g.157182390G>T , CM000664.1:g.157182390G>T	GRCh37
NC_000002.10:g.156890636G>T	NCBI36
NG_011821.1:g.11898C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1459C>A	ENSP00000514865.1:p.Leu487Met
ENST00000700229.1:c.627C>A
ENST00000700230.1:c.1203C>A	ENSP00000514867.1:n.1203C>A
ENST00000700231.1:c.1588C>A	ENSP00000514868.1:p.Leu530Met
ENST00000339562.9:c.1663C>A MANE Select	ENSP00000344479.4:p.Leu555Met
ENST00000675870.1:c.*174C>A	ENSP00000502739.1:n.*174C>A
ENST00000339562.8:c.1663C>A	ENSP00000344479.4:p.Leu555Met
ENST00000409108.6:c.1559C>A	ENSP00000386993.2:p.Thr520Asn
ENST00000409572.5:c.1663C>A	ENSP00000386747.1:p.Leu555Met
ENST00000417764.5:c.*174C>A	ENSP00000415632.1:n.*174C>A
ENST00000417972.5:c.*174C>A	ENSP00000394671.1:n.*174C>A
ENST00000426264.5:c.1474C>A	ENSP00000389986.1:p.Leu492Met
ENST00000429376.5:c.1370C>A	ENSP00000410952.1:p.Thr457Asn
NM_006186.3:c.1663C>A	NP_006177.1:p.Leu555Met
XM_005246621.2:c.1696C>A	XP_005246678.1:p.Leu566Met
XM_005246622.2:c.1474C>A	XP_005246679.1:p.Leu492Met
XM_005246623.1:c.1474C>A	XP_005246680.1:p.Leu492Met
XM_006712553.2:c.1621C>A	XP_006712616.1:p.Leu541Met
XM_011511246.1:c.1592C>A	XP_011509548.1:p.Thr531Asn
NM_173173.2:c.1474C>A	NP_775265.1:p.Leu492Met
XM_005246621.4:c.1696C>A	XP_005246678.1:p.Leu566Met
XM_006712553.4:c.1621C>A	XP_006712616.1:p.Leu541Met
XM_011511246.2:c.1592C>A	XP_011509548.1:p.Thr531Asn
XM_017004219.2:c.1663C>A	XP_016859708.1:p.Leu555Met
XM_017004220.2:c.1588C>A	XP_016859709.1:p.Leu530Met
XR_001738751.2:n.1910C>A
XR_001738752.2:n.1732C>A
XR_427087.4:n.1789C>A
NM_006186.4:c.1663C>A MANE Select	NP_006177.1:p.Leu555Met
NM_173173.3:c.1474C>A	NP_775265.1:p.Leu492Met