Canonical Allele Identifier: CA2246144775

Gene: ALOXE3

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8112131A= , CM000679.2:g.8112131A=	GRCh38
NC_000017.10:g.8015449A= , CM000679.1:g.8015449A=	GRCh37
NC_000017.9:g.7956174A=	NCBI36
NG_015807.1:g.11786T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318227.4:c.746T=	ENSP00000314879.4:p.Met249=
ENST00000380149.6:c.746T=	ENSP00000369494.2:p.Met249=
ENST00000448843.7:c.746T= MANE Select	ENSP00000400581.2:p.Met249=
ENST00000318227.3:c.1142T=	ENSP00000314879.3:p.Met381=
ENST00000380149.5:c.1214T=	ENSP00000369494.1:p.Met405=
ENST00000448843.6:c.746T=	ENSP00000400581.2:p.Met249=
NM_001165960.1:c.1142T=	NP_001159432.1:p.Met381=
NM_021628.2:c.746T=	NP_067641.2:p.Met249=
XM_017024921.2:c.746T=	XP_016880410.1:p.Met249=
XM_017024922.2:c.746T=	XP_016880411.1:p.Met249=
XM_017024923.2:c.746T=	XP_016880412.1:p.Met249=
XM_017024924.2:c.746T=	XP_016880413.1:p.Met249=
XM_017024925.2:c.746T=	XP_016880414.1:p.Met249=
XR_001752579.2:n.1019T=
XR_001752580.2:n.1019T=
NM_001369446.1:c.743T=	NP_001356375.1:p.Met248=
NM_021628.3:c.746T= MANE Select	NP_067641.2:p.Met249=