Canonical Allele Identifier: CA1300458944

Gene: NR4A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325986T= , CM000664.2:g.156325986T=	GRCh38
NC_000002.11:g.157182498T= , CM000664.1:g.157182498T=	GRCh37
NC_000002.10:g.156890744T=	NCBI36
NG_011821.1:g.11790A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.1351A=	ENSP00000514865.1:p.Lys451=
ENST00000700229.1:c.519A=
ENST00000700230.1:c.1095A=	ENSP00000514867.1:n.1095A=
ENST00000700231.1:c.1480A=	ENSP00000514868.1:p.Lys494=
ENST00000339562.9:c.1555A= MANE Select	ENSP00000344479.4:p.Lys519=
ENST00000675870.1:c.*66A=	ENSP00000502739.1:n.*66A=
ENST00000339562.8:c.1555A=	ENSP00000344479.4:p.Lys519=
ENST00000409108.6:c.1451A=	ENSP00000386993.2:p.Gln484=
ENST00000409572.5:c.1555A=	ENSP00000386747.1:p.Lys519=
ENST00000417764.5:c.*66A=	ENSP00000415632.1:n.*66A=
ENST00000417972.5:c.*66A=	ENSP00000394671.1:n.*66A=
ENST00000426264.5:c.1366A=	ENSP00000389986.1:p.Lys456=
ENST00000429376.5:c.1262A=	ENSP00000410952.1:p.Gln421=
NM_006186.3:c.1555A=	NP_006177.1:p.Lys519=
XM_005246621.2:c.1588A=	XP_005246678.1:p.Lys530=
XM_005246622.2:c.1366A=	XP_005246679.1:p.Lys456=
XM_005246623.1:c.1366A=	XP_005246680.1:p.Lys456=
XM_006712553.2:c.1513A=	XP_006712616.1:p.Lys505=
XM_011511246.1:c.1484A=	XP_011509548.1:p.Gln495=
XR_427087.2:n.3640A=
NM_173173.2:c.1366A=	NP_775265.1:p.Lys456=
XM_005246621.4:c.1588A=	XP_005246678.1:p.Lys530=
XM_006712553.4:c.1513A=	XP_006712616.1:p.Lys505=
XM_011511246.2:c.1484A=	XP_011509548.1:p.Gln495=
XM_017004219.2:c.1555A=	XP_016859708.1:p.Lys519=
XM_017004220.2:c.1480A=	XP_016859709.1:p.Lys494=
XR_001738751.2:n.1802A=
XR_001738752.2:n.1624A=
XR_427087.4:n.1681A=
NM_006186.4:c.1555A= MANE Select	NP_006177.1:p.Lys519=
NM_173173.3:c.1366A=	NP_775265.1:p.Lys456=