Canonical Allele Identifier: CA2244455751
Gene: ALOX15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631916C= , CM000679.2:g.4631916C= GRCh38
NC_000017.10:g.4535211C= , CM000679.1:g.4535211C= GRCh37
NC_000017.9:g.4481960C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.1782G= MANE Select ENSP00000293761.3:p.Trp594=
ENST00000570836.6:c.1782G= ENSP00000458832.1:p.Trp594=
ENST00000293761.7:c.1782G= ENSP00000293761.3:p.Trp594=
ENST00000570836.5:c.1782G= ENSP00000458832.1:p.Trp594=
ENST00000574640.1:c.1665G= ENSP00000460483.1:p.Trp555=
NM_001140.3:c.1782G= NP_001131.3:p.Trp594=
NM_001140.4:c.1782G= NP_001131.3:p.Trp594=
NM_001140.5:c.1782G= MANE Select NP_001131.3:p.Trp594=