Canonical Allele Identifier: CA2246144800

Gene: ALOXE3

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8112182T= , CM000679.2:g.8112182T=	GRCh38
NC_000017.10:g.8015500T= , CM000679.1:g.8015500T=	GRCh37
NC_000017.9:g.7956225T=	NCBI36
NG_015807.1:g.11735A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318227.4:c.695A=	ENSP00000314879.4:p.Lys232=
ENST00000380149.6:c.695A=	ENSP00000369494.2:p.Lys232=
ENST00000448843.7:c.695A= MANE Select	ENSP00000400581.2:p.Lys232=
ENST00000318227.3:c.1091A=	ENSP00000314879.3:p.Lys364=
ENST00000380149.5:c.1163A=	ENSP00000369494.1:p.Lys388=
ENST00000448843.6:c.695A=	ENSP00000400581.2:p.Lys232=
NM_001165960.1:c.1091A=	NP_001159432.1:p.Lys364=
NM_021628.2:c.695A=	NP_067641.2:p.Lys232=
XM_017024921.2:c.695A=	XP_016880410.1:p.Lys232=
XM_017024922.2:c.695A=	XP_016880411.1:p.Lys232=
XM_017024923.2:c.695A=	XP_016880412.1:p.Lys232=
XM_017024924.2:c.695A=	XP_016880413.1:p.Lys232=
XM_017024925.2:c.695A=	XP_016880414.1:p.Lys232=
XR_001752579.2:n.968A=
XR_001752580.2:n.968A=
NM_001369446.1:c.692A=	NP_001356375.1:p.Lys231=
NM_021628.3:c.695A= MANE Select	NP_067641.2:p.Lys232=