Canonical Allele Identifier: CA2246144767

Gene: ALOXE3

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8112103G= , CM000679.2:g.8112103G=	GRCh38
NC_000017.10:g.8015421G= , CM000679.1:g.8015421G=	GRCh37
NC_000017.9:g.7956146G=	NCBI36
NG_015807.1:g.11814C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318227.4:c.774C=	ENSP00000314879.4:p.Thr258=
ENST00000380149.6:c.774C=	ENSP00000369494.2:p.Thr258=
ENST00000448843.7:c.774C= MANE Select	ENSP00000400581.2:p.Thr258=
ENST00000318227.3:c.1170C=	ENSP00000314879.3:p.Thr390=
ENST00000380149.5:c.1242C=	ENSP00000369494.1:p.Thr414=
ENST00000448843.6:c.774C=	ENSP00000400581.2:p.Thr258=
NM_001165960.1:c.1170C=	NP_001159432.1:p.Thr390=
NM_021628.2:c.774C=	NP_067641.2:p.Thr258=
XM_017024921.2:c.774C=	XP_016880410.1:p.Thr258=
XM_017024922.2:c.774C=	XP_016880411.1:p.Thr258=
XM_017024923.2:c.774C=	XP_016880412.1:p.Thr258=
XM_017024924.2:c.774C=	XP_016880413.1:p.Thr258=
XM_017024925.2:c.774C=	XP_016880414.1:p.Thr258=
XR_001752579.2:n.1047C=
XR_001752580.2:n.1047C=
NM_001369446.1:c.771C=	NP_001356375.1:p.Thr257=
NM_021628.3:c.774C= MANE Select	NP_067641.2:p.Thr258=