Canonical Allele Identifier: CA397965087
Community Standard Title: NM_021628.3(ALOXE3):c.2065C>T (p.Arg689Trp)
Gene: ALOXE3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8096698G>A , CM000679.2:g.8096698G>A GRCh38
NC_000017.10:g.8000016G>A , CM000679.1:g.8000016G>A GRCh37
NC_000017.9:g.7940741G>A NCBI36
NG_015807.1:g.27219C>T

Transcript Alleles

HGVS Amino-acid Change
NM_021628.3:c.2065C>T MANE Select NP_067641.2:p.Arg689Trp
ENST00000448843.7:c.2065C>T MANE Select ENSP00000400581.2:p.Arg689Trp
NM_001165960.1:c.2461C>T NP_001159432.1:p.Arg821Trp
NM_001369446.1:c.2062C>T NP_001356375.1:p.Arg688Trp
NM_021628.2:c.2065C>T NP_067641.2:p.Arg689Trp
ENST00000318227.3:c.2461C>T ENSP00000314879.3:p.Arg821Trp
ENST00000318227.4:c.2065C>T ENSP00000314879.4:p.Arg689Trp
ENST00000380149.5:c.2533C>T ENSP00000369494.1:p.Arg845Trp
ENST00000380149.6:c.2065C>T ENSP00000369494.2:p.Arg689Trp
ENST00000448843.6:c.2065C>T ENSP00000400581.2:p.Arg689Trp
ENST00000583808.1:n.302C>T
XR_001752579.2:n.2216C>T
XR_001752580.2:n.2127C>T