Canonical Allele Identifier: CA2576161468

Gene: ALOXE3

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8112120_8112122del , CM000679.2:g.8112120_8112122del	GRCh38
NC_000017.10:g.8015438_8015440del , CM000679.1:g.8015438_8015440del	GRCh37
NC_000017.9:g.7956163_7956165del	NCBI36
NG_015807.1:g.11798_11800del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318227.4:c.758_760del	ENSP00000314879.4:p.Phe253del
ENST00000380149.6:c.758_760del	ENSP00000369494.2:p.Phe253del
ENST00000448843.7:c.758_760del MANE Select	ENSP00000400581.2:p.Phe253del
ENST00000318227.3:c.1154_1156del	ENSP00000314879.3:p.Phe385del
ENST00000380149.5:c.1226_1228del	ENSP00000369494.1:p.Phe409del
ENST00000448843.6:c.758_760del	ENSP00000400581.2:p.Phe253del
NM_001165960.1:c.1154_1156del	NP_001159432.1:p.Phe385del
NM_021628.2:c.758_760del	NP_067641.2:p.Phe253del
XM_017024921.2:c.758_760del	XP_016880410.1:p.Phe253del
XM_017024922.2:c.758_760del	XP_016880411.1:p.Phe253del
XM_017024923.2:c.758_760del	XP_016880412.1:p.Phe253del
XM_017024924.2:c.758_760del	XP_016880413.1:p.Phe253del
XM_017024925.2:c.758_760del	XP_016880414.1:p.Phe253del
XR_001752579.2:n.1031_1033del
XR_001752580.2:n.1031_1033del
NM_001369446.1:c.755_757del	NP_001356375.1:p.Phe252del
NM_021628.3:c.758_760del MANE Select	NP_067641.2:p.Phe253del