Canonical Allele Identifier: CA1867570656

Gene: NR4A3

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.99865020A= , CM000671.2:g.99865020A=	GRCh38
NC_000009.11:g.102627302A= , CM000671.1:g.102627302A=	GRCh37
NC_000009.10:g.101667123A=	NCBI36
NG_028910.1:g.48166A=

Transcript Alleles

HGVS	Amino-acid Change
NM_006981.4:c.*1153A= MANE Select	NP_008912.2:n.*1153A=
ENST00000395097.7:c.*1153A= MANE Select	ENSP00000378531.2:n.*1153A=
NM_006981.3:c.*1153A=	NP_008912.2:n.*1153A=
NM_173200.2:c.*1153A=	NP_775292.1:n.*1153A=
NM_173200.3:c.*1153A=	NP_775292.1:n.*1153A=
ENST00000330847.1:c.*1153A=	ENSP00000333122.1:n.*1153A=
ENST00000395097.6:c.*1153A=	ENSP00000378531.2:n.*1153A=
ENST00000618101.4:c.*1153A=	ENSP00000482027.1:n.*1153A=
XM_011519048.1:c.*1153A=	XP_011517350.1:n.*1153A=
XM_011519049.1:c.*1153A=	XP_011517351.1:n.*1153A=
XM_017015162.1:c.*1153A=	XP_016870651.1:n.*1153A=