Canonical Allele Identifier: CA2635534987
Gene: ALOX15 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631499_4631516dup , CM000679.2:g.4631499_4631516dup GRCh38
NC_000017.10:g.4534794_4534811dup , CM000679.1:g.4534794_4534811dup GRCh37
NC_000017.9:g.4481543_4481560dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.*95_*112dup MANE Select ENSP00000293761.3:n.*95_*112dup
ENST00000570836.6:c.*95_*112dup ENSP00000458832.1:n.*95_*112dup
ENST00000293761.7:c.*95_*112dup ENSP00000293761.3:n.*95_*112dup
ENST00000570836.5:c.*95_*112dup ENSP00000458832.1:n.*95_*112dup
ENST00000574640.1:c.*95_*112dup ENSP00000460483.1:n.*95_*112dup
NM_001140.3:c.*95_*112dup NP_001131.3:n.*95_*112dup
NM_001140.4:c.*95_*112dup NP_001131.3:n.*95_*112dup
NM_001140.5:c.*95_*112dup MANE Select NP_001131.3:n.*95_*112dup