Canonical Allele Identifier: CA1867576795

Gene: NR4A3

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.99823263T= , CM000671.2:g.99823263T=	GRCh38
NC_000009.11:g.102585545T= , CM000671.1:g.102585545T=	GRCh37
NC_000009.10:g.101625366T=	NCBI36
NG_028910.1:g.6409T=

Transcript Alleles

HGVS	Amino-acid Change
NM_006981.4:c.-177+856T= MANE Select	NP_008912.2:n.-177+856T=
ENST00000395097.7:c.-177+856T= MANE Select	ENSP00000378531.2:n.-177+856T=
NM_006981.3:c.-177+856T=	NP_008912.2:n.-177+856T=
NM_173199.2:c.-177+856T=	NP_775291.1:n.-177+856T=
NM_173199.3:c.-177+856T=	NP_775291.1:n.-177+856T=
NM_173199.4:c.-177+856T=	NP_775291.1:n.-177+856T=
NM_173200.2:c.-216+856T=	NP_775292.1:n.-216+856T=
NM_173200.3:c.-216+856T=	NP_775292.1:n.-216+856T=
ENST00000338488.8:c.-177+856T=	ENSP00000340301.4:n.-177+856T=
ENST00000395097.6:c.-177+856T=	ENSP00000378531.2:n.-177+856T=
ENST00000618101.4:c.-216+856T=	ENSP00000482027.1:n.-216+856T=
XM_005252237.2:c.-216+856T=	XP_005252294.1:n.-216+856T=
XM_011519048.1:c.-296+856T=	XP_011517350.1:n.-296+856T=