Canonical Allele Identifier: CA2244455378
Gene: ALOX15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631151C= , CM000679.2:g.4631151C= GRCh38
NC_000017.10:g.4534446C= , CM000679.1:g.4534446C= GRCh37
NC_000017.9:g.4481195C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.*449G= MANE Select ENSP00000293761.3:n.*449G=
ENST00000293761.7:c.*449G= ENSP00000293761.3:n.*449G=
ENST00000570836.5:c.*449G= ENSP00000458832.1:n.*449G=
NM_001140.3:c.*449G= NP_001131.3:n.*449G=
NM_001140.4:c.*449G= NP_001131.3:n.*449G=
NM_001140.5:c.*449G= MANE Select NP_001131.3:n.*449G=