Canonical Allele Identifier: CA397976596

Gene: ALOXE3

Linked Data

• MyVariant Identifiers: chr17:g.8015456C>T (hg19) ; chr17:g.8112138C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8112138C>T , CM000679.2:g.8112138C>T	GRCh38
NC_000017.10:g.8015456C>T , CM000679.1:g.8015456C>T	GRCh37
NC_000017.9:g.7956181C>T	NCBI36
NG_015807.1:g.11779G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318227.4:c.739G>A	ENSP00000314879.4:p.Asp247Asn
ENST00000380149.6:c.739G>A	ENSP00000369494.2:p.Asp247Asn
ENST00000448843.7:c.739G>A MANE Select	ENSP00000400581.2:p.Asp247Asn
ENST00000318227.3:c.1135G>A	ENSP00000314879.3:p.Asp379Asn
ENST00000380149.5:c.1207G>A	ENSP00000369494.1:p.Asp403Asn
ENST00000448843.6:c.739G>A	ENSP00000400581.2:p.Asp247Asn
NM_001165960.1:c.1135G>A	NP_001159432.1:p.Asp379Asn
NM_021628.2:c.739G>A	NP_067641.2:p.Asp247Asn
XM_017024921.2:c.739G>A	XP_016880410.1:p.Asp247Asn
XM_017024922.2:c.739G>A	XP_016880411.1:p.Asp247Asn
XM_017024923.2:c.739G>A	XP_016880412.1:p.Asp247Asn
XM_017024924.2:c.739G>A	XP_016880413.1:p.Asp247Asn
XM_017024925.2:c.739G>A	XP_016880414.1:p.Asp247Asn
XR_001752579.2:n.1012G>A
XR_001752580.2:n.1012G>A
NM_001369446.1:c.736G>A	NP_001356375.1:p.Asp246Asn
NM_021628.3:c.739G>A MANE Select	NP_067641.2:p.Asp247Asn