Canonical Allele Identifier: CA980964833
Gene: ALOX15 HGNC NCBI

Linked Data

dbSNP Id: rs1567645819

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631373_4631374del , CM000679.2:g.4631373_4631374del GRCh38
NC_000017.10:g.4534668_4534669del , CM000679.1:g.4534668_4534669del GRCh37
NC_000017.9:g.4481417_4481418del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.*234_*235del MANE Select ENSP00000293761.3:n.*234_*235del
ENST00000293761.7:c.*234_*235del ENSP00000293761.3:n.*234_*235del
ENST00000570836.5:c.*234_*235del ENSP00000458832.1:n.*234_*235del
ENST00000574640.1:c.*234_*235del ENSP00000460483.1:n.*234_*235del
NM_001140.3:c.*234_*235del NP_001131.3:n.*234_*235del
NM_001140.4:c.*234_*235del NP_001131.3:n.*234_*235del
NM_001140.5:c.*234_*235del MANE Select NP_001131.3:n.*234_*235del