Canonical Allele Identifier: CA287132901
Gene: ALOX15 HGNC NCBI

Linked Data

dbSNP Id: rs1040815472
gnomAD v3: 17-4631487-GGAGGGTGGGACATGGGAA-G
gnomAD v4: 17-4631487-GGAGGGTGGGACATGGGAA-G
MyVariant Identifiers: chr17:g.4534783_4534800del (hg19) chr17:g.4631488_4631505del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631499_4631516del , CM000679.2:g.4631499_4631516del GRCh38
NC_000017.10:g.4534794_4534811del , CM000679.1:g.4534794_4534811del GRCh37
NC_000017.9:g.4481543_4481560del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.*95_*112del MANE Select ENSP00000293761.3:n.*95_*112del
ENST00000570836.6:c.*95_*112del ENSP00000458832.1:n.*95_*112del
ENST00000293761.7:c.*95_*112del ENSP00000293761.3:n.*95_*112del
ENST00000570836.5:c.*95_*112del ENSP00000458832.1:n.*95_*112del
ENST00000574640.1:c.*95_*112del ENSP00000460483.1:n.*95_*112del
NM_001140.3:c.*95_*112del NP_001131.3:n.*95_*112del
NM_001140.4:c.*95_*112del NP_001131.3:n.*95_*112del
NM_001140.5:c.*95_*112del MANE Select NP_001131.3:n.*95_*112del
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