Canonical Allele Identifier: CA2244455397
Gene: ALOX15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631196C= , CM000679.2:g.4631196C= GRCh38
NC_000017.10:g.4534491C= , CM000679.1:g.4534491C= GRCh37
NC_000017.9:g.4481240C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.*404G= MANE Select ENSP00000293761.3:n.*404G=
ENST00000293761.7:c.*404G= ENSP00000293761.3:n.*404G=
ENST00000570836.5:c.*404G= ENSP00000458832.1:n.*404G=
NM_001140.3:c.*404G= NP_001131.3:n.*404G=
NM_001140.4:c.*404G= NP_001131.3:n.*404G=
NM_001140.5:c.*404G= MANE Select NP_001131.3:n.*404G=