Canonical Allele Identifier: CA2244455753
Gene: ALOX15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631925G= , CM000679.2:g.4631925G= GRCh38
NC_000017.10:g.4535220G= , CM000679.1:g.4535220G= GRCh37
NC_000017.9:g.4481969G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.1773C= MANE Select ENSP00000293761.3:p.Ser591=
ENST00000570836.6:c.1773C= ENSP00000458832.1:p.Ser591=
ENST00000293761.7:c.1773C= ENSP00000293761.3:p.Ser591=
ENST00000570836.5:c.1773C= ENSP00000458832.1:p.Ser591=
ENST00000574640.1:c.1656C= ENSP00000460483.1:p.Ser552=
NM_001140.3:c.1773C= NP_001131.3:p.Ser591=
NM_001140.4:c.1773C= NP_001131.3:p.Ser591=
NM_001140.5:c.1773C= MANE Select NP_001131.3:p.Ser591=