Canonical Allele Identifier: CA2244455552
Gene: ALOX15 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631500T= , CM000679.2:g.4631500T= GRCh38
NC_000017.10:g.4534795T= , CM000679.1:g.4534795T= GRCh37
NC_000017.9:g.4481544T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.*100A= MANE Select ENSP00000293761.3:n.*100A=
ENST00000570836.6:c.*100A= ENSP00000458832.1:n.*100A=
ENST00000293761.7:c.*100A= ENSP00000293761.3:n.*100A=
ENST00000570836.5:c.*100A= ENSP00000458832.1:n.*100A=
ENST00000574640.1:c.*100A= ENSP00000460483.1:n.*100A=
NM_001140.3:c.*100A= NP_001131.3:n.*100A=
NM_001140.4:c.*100A= NP_001131.3:n.*100A=
NM_001140.5:c.*100A= MANE Select NP_001131.3:n.*100A=
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