Canonical Allele Identifier: CA2635535743
Gene: ALOX15 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4636107_4636112dup , CM000679.2:g.4636107_4636112dup GRCh38
NC_000017.10:g.4539402_4539407dup , CM000679.1:g.4539402_4539407dup GRCh37
NC_000017.9:g.4486151_4486156dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.952-143_952-138dup MANE Select ENSP00000293761.3:n.952-143_952-138dup
ENST00000570836.6:c.952-143_952-138dup ENSP00000458832.1:n.952-143_952-138dup
ENST00000293761.7:c.952-143_952-138dup ENSP00000293761.3:n.952-143_952-138dup
ENST00000570836.5:c.952-143_952-138dup ENSP00000458832.1:n.952-143_952-138dup
ENST00000574640.1:c.835-143_835-138dup ENSP00000460483.1:n.835-143_835-138dup
NM_001140.3:c.952-143_952-138dup NP_001131.3:n.952-143_952-138dup
NM_001140.4:c.952-143_952-138dup NP_001131.3:n.952-143_952-138dup
NM_001140.5:c.952-143_952-138dup MANE Select NP_001131.3:n.952-143_952-138dup