Canonical Allele Identifier: CA772437263
Gene: ALOX15 HGNC NCBI

Linked Data

dbSNP Id: rs1422265887
gnomAD v3: 17-4631375-GAAGGAAGATAGGA-G
gnomAD v4: 17-4631375-GAAGGAAGATAGGA-G
MyVariant Identifiers: chr17:g.4534671_4534683del (hg19) chr17:g.4631376_4631388del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631381_4631393del , CM000679.2:g.4631381_4631393del GRCh38
NC_000017.10:g.4534676_4534688del , CM000679.1:g.4534676_4534688del GRCh37
NC_000017.9:g.4481425_4481437del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.*212_*224del MANE Select ENSP00000293761.3:n.*212_*224del
ENST00000293761.7:c.*212_*224del ENSP00000293761.3:n.*212_*224del
ENST00000570836.5:c.*212_*224del ENSP00000458832.1:n.*212_*224del
ENST00000574640.1:c.*212_*224del ENSP00000460483.1:n.*212_*224del
NM_001140.3:c.*212_*224del NP_001131.3:n.*212_*224del
NM_001140.4:c.*212_*224del NP_001131.3:n.*212_*224del
NM_001140.5:c.*212_*224del MANE Select NP_001131.3:n.*212_*224del
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