Canonical Allele Identifier: CA2635535099
Gene: ALOX15 HGNC NCBI

Linked Data

gnomAD v4: 17-4632003-CG-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4632008del , CM000679.2:g.4632008del GRCh38
NC_000017.10:g.4535303del , CM000679.1:g.4535303del GRCh37
NC_000017.9:g.4482052del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.1694del MANE Select ENSP00000293761.3:p.Pro565ArgfsTer12
ENST00000570836.6:c.1694del ENSP00000458832.1:p.Pro565ArgfsTer12
ENST00000293761.7:c.1694del ENSP00000293761.3:p.Pro565ArgfsTer12
ENST00000570836.5:c.1694del ENSP00000458832.1:p.Pro565ArgfsTer12
ENST00000574640.1:c.1577del ENSP00000460483.1:p.Pro526ArgfsTer12
NM_001140.3:c.1694del NP_001131.3:p.Pro565ArgfsTer12
NM_001140.4:c.1694del NP_001131.3:p.Pro565ArgfsTer12
NM_001140.5:c.1694del MANE Select NP_001131.3:p.Pro565ArgfsTer12
Search 100 bp 5'
Search 100 bp 3'