Canonical Allele Identifier: CA2244457876
Gene: ALOX15 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4636028G= , CM000679.2:g.4636028G= GRCh38
NC_000017.10:g.4539323G= , CM000679.1:g.4539323G= GRCh37
NC_000017.9:g.4486072G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.952-60C= MANE Select ENSP00000293761.3:n.952-60C=
ENST00000570836.6:c.952-60C= ENSP00000458832.1:n.952-60C=
ENST00000293761.7:c.952-60C= ENSP00000293761.3:n.952-60C=
ENST00000570836.5:c.952-60C= ENSP00000458832.1:n.952-60C=
ENST00000574640.1:c.835-60C= ENSP00000460483.1:n.835-60C=
NM_001140.3:c.952-60C= NP_001131.3:n.952-60C=
NM_001140.4:c.952-60C= NP_001131.3:n.952-60C=
NM_001140.5:c.952-60C= MANE Select NP_001131.3:n.952-60C=
Search 100 bp 5'
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