Canonical Allele Identifier: CA287132837
Gene: ALOX15 HGNC NCBI

Linked Data

dbSNP Id: rs11568132
gnomAD v2: 17-4534585-T-TCC
gnomAD v3: 17-4631290-T-TCC
gnomAD v4: 17-4631290-T-TCC
MyVariant Identifiers: chr17:g.4534585_4534586insCC (hg19) chr17:g.4631290_4631291insCC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631294_4631295dup , CM000679.2:g.4631294_4631295dup GRCh38
NC_000017.10:g.4534589_4534590dup , CM000679.1:g.4534589_4534590dup GRCh37
NC_000017.9:g.4481338_4481339dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.*308_*309dup MANE Select ENSP00000293761.3:n.*308_*309dup
ENST00000293761.7:c.*308_*309dup ENSP00000293761.3:n.*308_*309dup
ENST00000570836.5:c.*308_*309dup ENSP00000458832.1:n.*308_*309dup
NM_001140.3:c.*308_*309dup NP_001131.3:n.*308_*309dup
NM_001140.4:c.*308_*309dup NP_001131.3:n.*308_*309dup
NM_001140.5:c.*308_*309dup MANE Select NP_001131.3:n.*308_*309dup
Search 100 bp 5'
Search 100 bp 3'