Canonical Allele Identifier: CA2244455445
Gene: ALOX15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631316T= , CM000679.2:g.4631316T= GRCh38
NC_000017.10:g.4534611T= , CM000679.1:g.4534611T= GRCh37
NC_000017.9:g.4481360T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.*284A= MANE Select ENSP00000293761.3:n.*284A=
ENST00000293761.7:c.*284A= ENSP00000293761.3:n.*284A=
ENST00000570836.5:c.*284A= ENSP00000458832.1:n.*284A=
NM_001140.3:c.*284A= NP_001131.3:n.*284A=
NM_001140.4:c.*284A= NP_001131.3:n.*284A=
NM_001140.5:c.*284A= MANE Select NP_001131.3:n.*284A=