Canonical Allele Identifier: CA1867556222

Gene: NR4A3

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.99851390T= , CM000671.2:g.99851390T=	GRCh38
NC_000009.11:g.102613672T= , CM000671.1:g.102613672T=	GRCh37
NC_000009.10:g.101653493T=	NCBI36
NG_028910.1:g.34536T=

Transcript Alleles

HGVS	Amino-acid Change
NM_006981.4:c.1633+3775T= MANE Select	NP_008912.2:n.1633+3775T=
ENST00000395097.7:c.1633+3775T= MANE Select	ENSP00000378531.2:n.1633+3775T=
NM_006981.3:c.1633+3775T=	NP_008912.2:n.1633+3775T=
NM_173200.2:c.1666+3775T=	NP_775292.1:n.1666+3775T=
NM_173200.3:c.1666+3775T=	NP_775292.1:n.1666+3775T=
ENST00000330847.1:c.1666+3775T=	ENSP00000333122.1:n.1666+3775T=
ENST00000395097.6:c.1633+3775T=	ENSP00000378531.2:n.1633+3775T=
ENST00000618101.4:c.1666+3775T=	ENSP00000482027.1:n.1666+3775T=
XM_011519048.1:c.1633+3775T=	XP_011517350.1:n.1633+3775T=
XM_011519049.1:c.1633+3775T=	XP_011517351.1:n.1633+3775T=
XM_017015162.1:c.1633+3775T=	XP_016870651.1:n.1633+3775T=