Canonical Allele Identifier: CA2246144798

Gene: ALOXE3

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8112179A= , CM000679.2:g.8112179A=	GRCh38
NC_000017.10:g.8015497A= , CM000679.1:g.8015497A=	GRCh37
NC_000017.9:g.7956222A=	NCBI36
NG_015807.1:g.11738T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318227.4:c.698T=	ENSP00000314879.4:p.Leu233=
ENST00000380149.6:c.698T=	ENSP00000369494.2:p.Leu233=
ENST00000448843.7:c.698T= MANE Select	ENSP00000400581.2:p.Leu233=
ENST00000318227.3:c.1094T=	ENSP00000314879.3:p.Leu365=
ENST00000380149.5:c.1166T=	ENSP00000369494.1:p.Leu389=
ENST00000448843.6:c.698T=	ENSP00000400581.2:p.Leu233=
NM_001165960.1:c.1094T=	NP_001159432.1:p.Leu365=
NM_021628.2:c.698T=	NP_067641.2:p.Leu233=
XM_017024921.2:c.698T=	XP_016880410.1:p.Leu233=
XM_017024922.2:c.698T=	XP_016880411.1:p.Leu233=
XM_017024923.2:c.698T=	XP_016880412.1:p.Leu233=
XM_017024924.2:c.698T=	XP_016880413.1:p.Leu233=
XM_017024925.2:c.698T=	XP_016880414.1:p.Leu233=
XR_001752579.2:n.971T=
XR_001752580.2:n.971T=
NM_001369446.1:c.695T=	NP_001356375.1:p.Leu232=
NM_021628.3:c.698T= MANE Select	NP_067641.2:p.Leu233=