Canonical Allele Identifier: CA2244455394
Gene: ALOX15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631184A= , CM000679.2:g.4631184A= GRCh38
NC_000017.10:g.4534479A= , CM000679.1:g.4534479A= GRCh37
NC_000017.9:g.4481228A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.*416T= MANE Select ENSP00000293761.3:n.*416T=
ENST00000293761.7:c.*416T= ENSP00000293761.3:n.*416T=
ENST00000570836.5:c.*416T= ENSP00000458832.1:n.*416T=
NM_001140.3:c.*416T= NP_001131.3:n.*416T=
NM_001140.4:c.*416T= NP_001131.3:n.*416T=
NM_001140.5:c.*416T= MANE Select NP_001131.3:n.*416T=