Canonical Allele Identifier: CA2635936200

Gene: ALOXE3

Linked Data

• gnomAD v4: 17-8112071-TCTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8112074_8112076del , CM000679.2:g.8112074_8112076del	GRCh38
NC_000017.10:g.8015392_8015394del , CM000679.1:g.8015392_8015394del	GRCh37
NC_000017.9:g.7956117_7956119del	NCBI36
NG_015807.1:g.11843_11845del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318227.4:c.784+19_784+21del	ENSP00000314879.4:n.784+19_784+21del
ENST00000380149.6:c.784+19_784+21del	ENSP00000369494.2:n.784+19_784+21del
ENST00000448843.7:c.784+19_784+21del MANE Select	ENSP00000400581.2:n.784+19_784+21del
ENST00000318227.3:c.1180+19_1180+21del	ENSP00000314879.3:n.1180+19_1180+21del
ENST00000380149.5:c.1252+19_1252+21del	ENSP00000369494.1:n.1252+19_1252+21del
ENST00000448843.6:c.784+19_784+21del	ENSP00000400581.2:n.784+19_784+21del
NM_001165960.1:c.1180+19_1180+21del	NP_001159432.1:n.1180+19_1180+21del
NM_021628.2:c.784+19_784+21del	NP_067641.2:n.784+19_784+21del
XM_017024921.2:c.784+19_784+21del	XP_016880410.1:n.784+19_784+21del
XM_017024922.2:c.784+19_784+21del	XP_016880411.1:n.784+19_784+21del
XM_017024923.2:c.784+19_784+21del	XP_016880412.1:n.784+19_784+21del
XM_017024924.2:c.784+19_784+21del	XP_016880413.1:n.784+19_784+21del
XM_017024925.2:c.784+19_784+21del	XP_016880414.1:n.784+19_784+21del
XR_001752579.2:n.1057+19_1057+21del
XR_001752580.2:n.1057+19_1057+21del
NM_001369446.1:c.781+19_781+21del	NP_001356375.1:n.781+19_781+21del
NM_021628.3:c.784+19_784+21del MANE Select	NP_067641.2:n.784+19_784+21del