Canonical Allele Identifier: CA2635535098
Gene: ALOX15 HGNC NCBI

Linked Data

gnomAD v4: 17-4632002-GC-G
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4632003del , CM000679.2:g.4632003del GRCh38
NC_000017.10:g.4535298del , CM000679.1:g.4535298del GRCh37
NC_000017.9:g.4482047del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.1695del MANE Select ENSP00000293761.3:p.Pro566GlnfsTer11
ENST00000570836.6:c.1695del ENSP00000458832.1:p.Pro566GlnfsTer11
ENST00000293761.7:c.1695del ENSP00000293761.3:p.Pro566GlnfsTer11
ENST00000570836.5:c.1695del ENSP00000458832.1:p.Pro566GlnfsTer11
ENST00000574640.1:c.1578del ENSP00000460483.1:p.Pro527GlnfsTer11
NM_001140.3:c.1695del NP_001131.3:p.Pro566GlnfsTer11
NM_001140.4:c.1695del NP_001131.3:p.Pro566GlnfsTer11
NM_001140.5:c.1695del MANE Select NP_001131.3:p.Pro566GlnfsTer11
Search 100 bp 5'
Search 100 bp 3'