Canonical Allele Identifier: CA2244455384
Gene: ALOX15 HGNC NCBI

Linked Data

dbSNP Id: rs1910880811

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631174_4631175dup , CM000679.2:g.4631174_4631175dup GRCh38
NC_000017.10:g.4534469_4534470dup , CM000679.1:g.4534469_4534470dup GRCh37
NC_000017.9:g.4481218_4481219dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.*426_*427dup MANE Select ENSP00000293761.3:n.*426_*427dup
ENST00000293761.7:c.*426_*427dup ENSP00000293761.3:n.*426_*427dup
ENST00000570836.5:c.*426_*427dup ENSP00000458832.1:n.*426_*427dup
NM_001140.3:c.*426_*427dup NP_001131.3:n.*426_*427dup
NM_001140.4:c.*426_*427dup NP_001131.3:n.*426_*427dup
NM_001140.5:c.*426_*427dup MANE Select NP_001131.3:n.*426_*427dup