Canonical Allele Identifier: CA348680027

Gene: NR4A2

Linked Data

• MyVariant Identifiers: chr2:g.157182698C>A (hg19) ; chr2:g.156326186C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156326186C>A , CM000664.2:g.156326186C>A	GRCh38
NC_000002.11:g.157182698C>A , CM000664.1:g.157182698C>A	GRCh37
NC_000002.10:g.156890944C>A	NCBI36
NG_011821.1:g.11590G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1300G>T	ENSP00000514865.1:p.Ala434Ser
ENST00000700229.1:c.468G>T
ENST00000700230.1:c.1044G>T	ENSP00000514867.1:n.1044G>T
ENST00000700231.1:c.1429G>T	ENSP00000514868.1:p.Ala477Ser
ENST00000339562.9:c.1504G>T MANE Select	ENSP00000344479.4:p.Ala502Ser
ENST00000675870.1:c.*15G>T	ENSP00000502739.1:n.*15G>T
ENST00000339562.8:c.1504G>T	ENSP00000344479.4:p.Ala502Ser
ENST00000409108.6:c.1400G>T	ENSP00000386993.2:p.Cys467Phe
ENST00000409572.5:c.1504G>T	ENSP00000386747.1:p.Ala502Ser
ENST00000417764.5:c.*15G>T	ENSP00000415632.1:n.*15G>T
ENST00000417972.5:c.*15G>T	ENSP00000394671.1:n.*15G>T
ENST00000426264.5:c.1315G>T	ENSP00000389986.1:p.Ala439Ser
ENST00000429376.5:c.1211G>T	ENSP00000410952.1:p.Cys404Phe
NM_006186.3:c.1504G>T	NP_006177.1:p.Ala502Ser
XM_005246621.2:c.1537G>T	XP_005246678.1:p.Ala513Ser
XM_005246622.2:c.1315G>T	XP_005246679.1:p.Ala439Ser
XM_005246623.1:c.1315G>T	XP_005246680.1:p.Ala439Ser
XM_006712553.2:c.1462G>T	XP_006712616.1:p.Ala488Ser
XM_011511246.1:c.1433G>T	XP_011509548.1:p.Cys478Phe
XR_427087.2:n.3589G>T
NM_173173.2:c.1315G>T	NP_775265.1:p.Ala439Ser
XM_005246621.4:c.1537G>T	XP_005246678.1:p.Ala513Ser
XM_006712553.4:c.1462G>T	XP_006712616.1:p.Ala488Ser
XM_011511246.2:c.1433G>T	XP_011509548.1:p.Cys478Phe
XM_017004219.2:c.1504G>T	XP_016859708.1:p.Ala502Ser
XM_017004220.2:c.1429G>T	XP_016859709.1:p.Ala477Ser
XR_001738751.2:n.1751G>T
XR_001738752.2:n.1573G>T
XR_427087.4:n.1630G>T
NM_006186.4:c.1504G>T MANE Select	NP_006177.1:p.Ala502Ser
NM_173173.3:c.1315G>T	NP_775265.1:p.Ala439Ser