Canonical Allele Identifier: CA8306700
Gene: ALOX15 HGNC NCBI

Linked Data

ClinVar Variation Id: 786301
ClinVar RCV Id: RCV000968337
dbSNP Id: rs147458306
ExAC: 17:4535298 C / T
gnomAD v2: 17-4535298-C-T
gnomAD v3: 17-4632003-C-T
gnomAD v4: 17-4632003-C-T
MyVariant Identifiers: chr17:g.4535298C>T (hg19) chr17:g.4632003C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4632003C>T , CM000679.2:g.4632003C>T GRCh38
NC_000017.10:g.4535298C>T , CM000679.1:g.4535298C>T GRCh37
NC_000017.9:g.4482047C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.1695G>A MANE Select ENSP00000293761.3:p.Pro565=
ENST00000570836.6:c.1695G>A ENSP00000458832.1:p.Pro565=
ENST00000293761.7:c.1695G>A ENSP00000293761.3:p.Pro565=
ENST00000570836.5:c.1695G>A ENSP00000458832.1:p.Pro565=
ENST00000574640.1:c.1578G>A ENSP00000460483.1:p.Pro526=
NM_001140.3:c.1695G>A NP_001131.3:p.Pro565=
NM_001140.4:c.1695G>A NP_001131.3:p.Pro565=
NM_001140.5:c.1695G>A MANE Select NP_001131.3:p.Pro565=
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Search 100 bp 3'