Canonical Allele Identifier: CA2246144839
Gene: ALOXE3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8112270C= , CM000679.2:g.8112270C= GRCh38
NC_000017.10:g.8015588C= , CM000679.1:g.8015588C= GRCh37
NC_000017.9:g.7956313C= NCBI36
NG_015807.1:g.11647G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000318227.4:c.681-74G= ENSP00000314879.4:n.681-74G=
ENST00000380149.6:c.681-74G= ENSP00000369494.2:n.681-74G=
ENST00000448843.7:c.681-74G= MANE Select ENSP00000400581.2:n.681-74G=
ENST00000318227.3:c.1077-74G= ENSP00000314879.3:n.1077-74G=
ENST00000380149.5:c.1149-74G= ENSP00000369494.1:n.1149-74G=
ENST00000448843.6:c.681-74G= ENSP00000400581.2:n.681-74G=
NM_001165960.1:c.1077-74G= NP_001159432.1:n.1077-74G=
NM_021628.2:c.681-74G= NP_067641.2:n.681-74G=
XM_017024921.2:c.681-74G= XP_016880410.1:n.681-74G=
XM_017024922.2:c.681-74G= XP_016880411.1:n.681-74G=
XM_017024923.2:c.681-74G= XP_016880412.1:n.681-74G=
XM_017024924.2:c.681-74G= XP_016880413.1:n.681-74G=
XM_017024925.2:c.681-74G= XP_016880414.1:n.681-74G=
XR_001752579.2:n.954-74G=
XR_001752580.2:n.954-74G=
NM_001369446.1:c.678-74G= NP_001356375.1:n.678-74G=
NM_021628.3:c.681-74G= MANE Select NP_067641.2:n.681-74G=