Canonical Allele Identifier: CA397973526

Gene: ALOXE3

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8110189T>C , CM000679.2:g.8110189T>C	GRCh38
NC_000017.10:g.8013507T>C , CM000679.1:g.8013507T>C	GRCh37
NC_000017.9:g.7954232T>C	NCBI36
NG_015807.1:g.13728A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_021628.3:c.1208A>G MANE Select	NP_067641.2:p.His403Arg
ENST00000448843.7:c.1208A>G MANE Select	ENSP00000400581.2:p.His403Arg
NM_001165960.1:c.1604A>G	NP_001159432.1:p.His535Arg
NM_001369446.1:c.1205A>G	NP_001356375.1:p.His402Arg
NM_021628.2:c.1208A>G	NP_067641.2:p.His403Arg
ENST00000318227.3:c.1604A>G	ENSP00000314879.3:p.His535Arg
ENST00000318227.4:c.1208A>G	ENSP00000314879.4:p.His403Arg
ENST00000380149.5:c.1676A>G	ENSP00000369494.1:p.His559Arg
ENST00000380149.6:c.1208A>G	ENSP00000369494.2:p.His403Arg
ENST00000448843.6:c.1208A>G	ENSP00000400581.2:p.His403Arg
XM_017024921.2:c.1208A>G	XP_016880410.1:p.His403Arg
XM_017024922.2:c.1208A>G	XP_016880411.1:p.His403Arg
XM_017024923.2:c.1208A>G	XP_016880412.1:p.His403Arg
XM_017024924.2:c.1208A>G	XP_016880413.1:p.His403Arg
XM_017024925.2:c.1208A>G	XP_016880414.1:p.His403Arg
XR_001752579.2:n.1481A>G
XR_001752580.2:n.1481A>G