Canonical Allele Identifier: CA287132822
Gene: ALOX15 HGNC NCBI

Linked Data

dbSNP Id: rs200868987
gnomAD v2: 17-4534526-TAAC-T
gnomAD v3: 17-4631231-TAAC-T
gnomAD v4: 17-4631231-TAAC-T
MyVariant Identifiers: chr17:g.4534527_4534529del (hg19) chr17:g.4631232_4631234del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631240_4631242del , CM000679.2:g.4631240_4631242del GRCh38
NC_000017.10:g.4534535_4534537del , CM000679.1:g.4534535_4534537del GRCh37
NC_000017.9:g.4481284_4481286del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.*366_*368del MANE Select ENSP00000293761.3:n.*366_*368del
ENST00000293761.7:c.*366_*368del ENSP00000293761.3:n.*366_*368del
ENST00000570836.5:c.*366_*368del ENSP00000458832.1:n.*366_*368del
NM_001140.3:c.*366_*368del NP_001131.3:n.*366_*368del
NM_001140.4:c.*366_*368del NP_001131.3:n.*366_*368del
NM_001140.5:c.*366_*368del MANE Select NP_001131.3:n.*366_*368del
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