Canonical Allele Identifier: CA8306603
Gene: ALOX15 HGNC NCBI

Linked Data

dbSNP Id: rs747060783
ExAC: 17:4534856 TGGGTGA / T
gnomAD v2: 17-4534856-TGGGTGA-T
gnomAD v4: 17-4631561-TGGGTGA-T
MyVariant Identifiers: chr17:g.4534857_4534862del (hg19) chr17:g.4631562_4631567del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631562_4631567del , CM000679.2:g.4631562_4631567del GRCh38
NC_000017.10:g.4534857_4534862del , CM000679.1:g.4534857_4534862del GRCh37
NC_000017.9:g.4481606_4481611del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000293761.8:c.*33_*38del MANE Select ENSP00000293761.3:n.*33_*38del
ENST00000570836.6:c.*33_*38del ENSP00000458832.1:n.*33_*38del
ENST00000293761.7:c.*33_*38del ENSP00000293761.3:n.*33_*38del
ENST00000570836.5:c.*33_*38del ENSP00000458832.1:n.*33_*38del
ENST00000574640.1:c.*33_*38del ENSP00000460483.1:n.*33_*38del
NM_001140.3:c.*33_*38del NP_001131.3:n.*33_*38del
NM_001140.4:c.*33_*38del NP_001131.3:n.*33_*38del
NM_001140.5:c.*33_*38del MANE Select NP_001131.3:n.*33_*38del
Search 100 bp 5'
Search 100 bp 3'