Canonical Allele Identifier: CA2244455519
Gene: ALOX15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631444T= , CM000679.2:g.4631444T= GRCh38
NC_000017.10:g.4534739T= , CM000679.1:g.4534739T= GRCh37
NC_000017.9:g.4481488T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000293761.8:c.*156A= MANE Select ENSP00000293761.3:n.*156A=
ENST00000293761.7:c.*156A= ENSP00000293761.3:n.*156A=
ENST00000570836.5:c.*156A= ENSP00000458832.1:n.*156A=
ENST00000574640.1:c.*156A= ENSP00000460483.1:n.*156A=
NM_001140.3:c.*156A= NP_001131.3:n.*156A=
NM_001140.4:c.*156A= NP_001131.3:n.*156A=
NM_001140.5:c.*156A= MANE Select NP_001131.3:n.*156A=