Canonical Allele Identifier: CA2244455399
Gene: ALOX15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631200C= , CM000679.2:g.4631200C= GRCh38
NC_000017.10:g.4534495C= , CM000679.1:g.4534495C= GRCh37
NC_000017.9:g.4481244C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.*400G= MANE Select ENSP00000293761.3:n.*400G=
ENST00000293761.7:c.*400G= ENSP00000293761.3:n.*400G=
ENST00000570836.5:c.*400G= ENSP00000458832.1:n.*400G=
NM_001140.3:c.*400G= NP_001131.3:n.*400G=
NM_001140.4:c.*400G= NP_001131.3:n.*400G=
NM_001140.5:c.*400G= MANE Select NP_001131.3:n.*400G=