Canonical Allele Identifier: CA2246144763
Gene: ALOXE3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8112096T= , CM000679.2:g.8112096T= GRCh38
NC_000017.10:g.8015414T= , CM000679.1:g.8015414T= GRCh37
NC_000017.9:g.7956139T= NCBI36
NG_015807.1:g.11821A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000318227.4:c.781A= ENSP00000314879.4:p.Thr261=
ENST00000380149.6:c.781A= ENSP00000369494.2:p.Thr261=
ENST00000448843.7:c.781A= MANE Select ENSP00000400581.2:p.Thr261=
ENST00000318227.3:c.1177A= ENSP00000314879.3:p.Thr393=
ENST00000380149.5:c.1249A= ENSP00000369494.1:p.Thr417=
ENST00000448843.6:c.781A= ENSP00000400581.2:p.Thr261=
NM_001165960.1:c.1177A= NP_001159432.1:p.Thr393=
NM_021628.2:c.781A= NP_067641.2:p.Thr261=
XM_017024921.2:c.781A= XP_016880410.1:p.Thr261=
XM_017024922.2:c.781A= XP_016880411.1:p.Thr261=
XM_017024923.2:c.781A= XP_016880412.1:p.Thr261=
XM_017024924.2:c.781A= XP_016880413.1:p.Thr261=
XM_017024925.2:c.781A= XP_016880414.1:p.Thr261=
XR_001752579.2:n.1054A=
XR_001752580.2:n.1054A=
NM_001369446.1:c.778A= NP_001356375.1:p.Thr260=
NM_021628.3:c.781A= MANE Select NP_067641.2:p.Thr261=