Canonical Allele Identifier: CA2244455493
Gene: ALOX15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631386G= , CM000679.2:g.4631386G= GRCh38
NC_000017.10:g.4534681G= , CM000679.1:g.4534681G= GRCh37
NC_000017.9:g.4481430G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.*214C= MANE Select ENSP00000293761.3:n.*214C=
ENST00000293761.7:c.*214C= ENSP00000293761.3:n.*214C=
ENST00000570836.5:c.*214C= ENSP00000458832.1:n.*214C=
ENST00000574640.1:c.*214C= ENSP00000460483.1:n.*214C=
NM_001140.3:c.*214C= NP_001131.3:n.*214C=
NM_001140.4:c.*214C= NP_001131.3:n.*214C=
NM_001140.5:c.*214C= MANE Select NP_001131.3:n.*214C=