Canonical Allele Identifier: CA2244455432
Gene: ALOX15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631286T= , CM000679.2:g.4631286T= GRCh38
NC_000017.10:g.4534581T= , CM000679.1:g.4534581T= GRCh37
NC_000017.9:g.4481330T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.*314A= MANE Select ENSP00000293761.3:n.*314A=
ENST00000293761.7:c.*314A= ENSP00000293761.3:n.*314A=
ENST00000570836.5:c.*314A= ENSP00000458832.1:n.*314A=
NM_001140.3:c.*314A= NP_001131.3:n.*314A=
NM_001140.4:c.*314A= NP_001131.3:n.*314A=
NM_001140.5:c.*314A= MANE Select NP_001131.3:n.*314A=