Canonical Allele Identifier: CA287132833
Gene: ALOX15 HGNC NCBI

Linked Data

dbSNP Id: rs149949350
gnomAD v2: 17-4534535-CAAA-C
gnomAD v3: 17-4631240-CAAA-C
gnomAD v4: 17-4631240-CAAA-C
MyVariant Identifiers: chr17:g.4534536_4534538del (hg19) chr17:g.4631241_4631243del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631245_4631247del , CM000679.2:g.4631245_4631247del GRCh38
NC_000017.10:g.4534540_4534542del , CM000679.1:g.4534540_4534542del GRCh37
NC_000017.9:g.4481289_4481291del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.*357_*359del MANE Select ENSP00000293761.3:n.*357_*359del
ENST00000293761.7:c.*357_*359del ENSP00000293761.3:n.*357_*359del
ENST00000570836.5:c.*357_*359del ENSP00000458832.1:n.*357_*359del
NM_001140.3:c.*357_*359del NP_001131.3:n.*357_*359del
NM_001140.4:c.*357_*359del NP_001131.3:n.*357_*359del
NM_001140.5:c.*357_*359del MANE Select NP_001131.3:n.*357_*359del
Search 100 bp 5'
Search 100 bp 3'