Canonical Allele Identifier: CA348680043

Gene: NR4A2

Linked Data

• MyVariant Identifiers: chr2:g.157182704T>A (hg19) ; chr2:g.156326192T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156326192T>A , CM000664.2:g.156326192T>A	GRCh38
NC_000002.11:g.157182704T>A , CM000664.1:g.157182704T>A	GRCh37
NC_000002.10:g.156890950T>A	NCBI36
NG_011821.1:g.11584A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1294A>T	ENSP00000514865.1:p.Ile432Phe
ENST00000700229.1:c.462A>T
ENST00000700230.1:c.1038A>T	ENSP00000514867.1:n.1038A>T
ENST00000700231.1:c.1423A>T	ENSP00000514868.1:p.Ile475Phe
ENST00000339562.9:c.1498A>T MANE Select	ENSP00000344479.4:p.Ile500Phe
ENST00000675870.1:c.*9A>T	ENSP00000502739.1:n.*9A>T
ENST00000339562.8:c.1498A>T	ENSP00000344479.4:p.Ile500Phe
ENST00000409108.6:c.1394A>T	ENSP00000386993.2:p.His465Leu
ENST00000409572.5:c.1498A>T	ENSP00000386747.1:p.Ile500Phe
ENST00000417764.5:c.*9A>T	ENSP00000415632.1:n.*9A>T
ENST00000417972.5:c.*9A>T	ENSP00000394671.1:n.*9A>T
ENST00000426264.5:c.1309A>T	ENSP00000389986.1:p.Ile437Phe
ENST00000429376.5:c.1205A>T	ENSP00000410952.1:p.His402Leu
NM_006186.3:c.1498A>T	NP_006177.1:p.Ile500Phe
XM_005246621.2:c.1531A>T	XP_005246678.1:p.Ile511Phe
XM_005246622.2:c.1309A>T	XP_005246679.1:p.Ile437Phe
XM_005246623.1:c.1309A>T	XP_005246680.1:p.Ile437Phe
XM_006712553.2:c.1456A>T	XP_006712616.1:p.Ile486Phe
XM_011511246.1:c.1427A>T	XP_011509548.1:p.His476Leu
XR_427087.2:n.3583A>T
NM_173173.2:c.1309A>T	NP_775265.1:p.Ile437Phe
XM_005246621.4:c.1531A>T	XP_005246678.1:p.Ile511Phe
XM_006712553.4:c.1456A>T	XP_006712616.1:p.Ile486Phe
XM_011511246.2:c.1427A>T	XP_011509548.1:p.His476Leu
XM_017004219.2:c.1498A>T	XP_016859708.1:p.Ile500Phe
XM_017004220.2:c.1423A>T	XP_016859709.1:p.Ile475Phe
XR_001738751.2:n.1745A>T
XR_001738752.2:n.1567A>T
XR_427087.4:n.1624A>T
NM_006186.4:c.1498A>T MANE Select	NP_006177.1:p.Ile500Phe
NM_173173.3:c.1309A>T	NP_775265.1:p.Ile437Phe