Canonical Allele Identifier: CA2635534729
Gene: ALOX15 HGNC NCBI

Linked Data

dbSNP Id: rs2150534122

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631172_4631197del , CM000679.2:g.4631172_4631197del GRCh38
NC_000017.10:g.4534467_4534492del , CM000679.1:g.4534467_4534492del GRCh37
NC_000017.9:g.4481216_4481241del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.*403_*428del MANE Select ENSP00000293761.3:n.*403_*428del
ENST00000293761.7:c.*403_*428del ENSP00000293761.3:n.*403_*428del
ENST00000570836.5:c.*403_*428del ENSP00000458832.1:n.*403_*428del
NM_001140.3:c.*403_*428del NP_001131.3:n.*403_*428del
NM_001140.4:c.*403_*428del NP_001131.3:n.*403_*428del
NM_001140.5:c.*403_*428del MANE Select NP_001131.3:n.*403_*428del