Canonical Allele Identifier: CA1867582106

Gene: NR4A3

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.99827383T= , CM000671.2:g.99827383T=	GRCh38
NC_000009.11:g.102589665T= , CM000671.1:g.102589665T=	GRCh37
NC_000009.10:g.101629486T=	NCBI36
NG_028910.1:g.10529T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395097.7:c.-2-658T= MANE Select	ENSP00000378531.2:n.-2-658T=
ENST00000330847.1:c.31+582T=	ENSP00000333122.1:n.31+582T=
ENST00000338488.8:c.-2-658T=	ENSP00000340301.4:n.-2-658T=
ENST00000395097.6:c.-2-658T=	ENSP00000378531.2:n.-2-658T=
ENST00000618101.4:c.31+582T=	ENSP00000482027.1:n.31+582T=
NM_006981.3:c.-2-658T=	NP_008912.2:n.-2-658T=
NM_173199.2:c.-2-658T=	NP_775291.1:n.-2-658T=
NM_173200.2:c.31+582T=	NP_775292.1:n.31+582T=
XM_005252237.2:c.31+582T=	XP_005252294.1:n.31+582T=
XM_011519048.1:c.-86T=	XP_011517350.1:n.-86T=
XM_011519049.1:c.-86T=	XP_011517351.1:n.-86T=
XM_017015162.1:c.-86T=	XP_016870651.1:n.-86T=
NM_006981.4:c.-2-658T= MANE Select	NP_008912.2:n.-2-658T=
NM_173199.3:c.-2-658T=	NP_775291.1:n.-2-658T=
NM_173199.4:c.-2-658T=	NP_775291.1:n.-2-658T=
NM_173200.3:c.31+582T=	NP_775292.1:n.31+582T=