Canonical Allele Identifier: CA2244455387
Gene: ALOX15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631177C= , CM000679.2:g.4631177C= GRCh38
NC_000017.10:g.4534472C= , CM000679.1:g.4534472C= GRCh37
NC_000017.9:g.4481221C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.*423G= MANE Select ENSP00000293761.3:n.*423G=
ENST00000293761.7:c.*423G= ENSP00000293761.3:n.*423G=
ENST00000570836.5:c.*423G= ENSP00000458832.1:n.*423G=
NM_001140.3:c.*423G= NP_001131.3:n.*423G=
NM_001140.4:c.*423G= NP_001131.3:n.*423G=
NM_001140.5:c.*423G= MANE Select NP_001131.3:n.*423G=