Canonical Allele Identifier: CA2244455528
Gene: ALOX15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631468T= , CM000679.2:g.4631468T= GRCh38
NC_000017.10:g.4534763T= , CM000679.1:g.4534763T= GRCh37
NC_000017.9:g.4481512T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000293761.8:c.*132A= MANE Select ENSP00000293761.3:n.*132A=
ENST00000293761.7:c.*132A= ENSP00000293761.3:n.*132A=
ENST00000570836.5:c.*132A= ENSP00000458832.1:n.*132A=
ENST00000574640.1:c.*132A= ENSP00000460483.1:n.*132A=
NM_001140.3:c.*132A= NP_001131.3:n.*132A=
NM_001140.4:c.*132A= NP_001131.3:n.*132A=
NM_001140.5:c.*132A= MANE Select NP_001131.3:n.*132A=